1-16 of about 16 matches for site:www.fda.gov foley catheter
Guidance for the Content of Premarket Notifications for Conventional and Antimicrobial Foley Cathete
https://www.fda.gov/regulatory-information/search-fda-guidance-documen...
and other applicable characteristics. FDA recommends that each premarket notification for a Foley catheter includes the
Guidance for the Content of Premarket Notifications for Conventional and Antimicrobial Foley Cathete
https://www.fda.gov/regulatory-information/search-fda-guidance-documen...
and other applicable characteristics. FDA recommends that each premarket notification for a Foley catheter includes the
https://www.fda.gov/medical-devices/medical-device-recalls/deroyal-ind...
DeRoyal Industries, Inc. Recalls Tracecarts Containing 16FR Urine Meter Foley Under Recall by Nurse Assist | FDA Skip to main
https://www.fda.gov/regulatory-information/search-fda-guidance-documen...
Cardiovascular Catheter Sheath Introducer Kit Cardiovascular Procedure Kit Cardiovascular Surgical Instruments Tray Catheter Balloon Repair Kit Catheter Guide Wire Kit Catheter
https://www.fda.gov/medical-devices/medical-device-connectors/examples...
with her Foley catheter disconnected from its drainage bag. One end of the catheter was still in
https://www.fda.gov/medical-devices/medical-device-recalls/2024-medica...
Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty 04/29
https://www.fda.gov/medical-devices/medical-device-safety#section-nav
Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty 04/29
https://www.fda.gov/medical-devices/medical-device-safety#main-content
Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty 04/29
https://www.fda.gov/medical-devices/medical-device-safety#search-form
Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty 04/29
https://www.fda.gov/medical-devices/medical-device-safety#footer-headi...
Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty 04/29
https://www.fda.gov/medical-devices/medical-devices-news-and-events/cd...
the FD&C Act April 25, 2024 Class I Recall: Fresenius Medical Care Recalls Stay-Safe Catheter Extension Sets and
https://www.fda.gov/medical-devices/medical-devices-news-and-events/cd...
the FD&C Act April 25, 2024 Class I Recall: Fresenius Medical Care Recalls Stay-Safe Catheter Extension Sets and
https://www.fda.gov/medical-devices/medical-devices-news-and-events/cd...
the FD&C Act April 25, 2024 Class I Recall: Fresenius Medical Care Recalls Stay-Safe Catheter Extension Sets and
https://www.fda.gov/medical-devices/medical-devices-news-and-events/cd...
the FD&C Act April 25, 2024 Class I Recall: Fresenius Medical Care Recalls Stay-Safe Catheter Extension Sets and
https://www.fda.gov/medical-devices/guidance-documents-medical-devices...
the Content of Premarket Notifications for Conventional and Antimicrobial Foley Catheters 510(k) Checklist
https://www.fda.gov/medical-devices/medical-device-safety
to a Software-Related Possible Power Malfunction 05/13/2024 Route 92 Medical Inc. Recalls Catheter due to Distal