FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CPR FOLEY CAHTETER KIT

K Number: K960214 · Decision Apr 1, 1996
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
59
Applicant Total
21
Review Days
76

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Basic Information

Device Name
CPR FOLEY CAHTETER KIT
K Number
K960214
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Custom Pack Reliability
Date Received
January 16, 1996
Decision Date
April 1, 1996
Product Code
FCM
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FCM), ordered by most recent decision date.

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Other Clearances by Custom Pack Reliability

K Number Device Name
K960205 CPR TRACHEOTOMY CARE TRAY
K960243 CPR C-SECTION DELIVERY PACK
K960239 CPR D & C TRAY
K960216 CPR SUCTION CATHETER KIT
K960211 CPR TOTAL KNEE PACK
K960210 CPR ORTHO HAND PACK
K960206 CPR DRESSING CHANGE TRAY
K960213 CPR TOTAL HIP PACK
K960209 CPR HEART PACK
K960212 CPR IRRIGATION TRAY
Search all 21 clearances from Custom Pack Reliability →