inforMED
PPBClass II

Foley Catheter Kit (excludes Hiv Testing)

Gastroenterology, Urology · 21 CFR 876.5130

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

MDR events91All time
Recalls14All time
Registered firms25Currently listed
510(k) clearances0All time

Recalls

14 recall events for this product code

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510(k) clearances

0 clearances for this product code

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No 510(k) clearances on file for this product code.