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

KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET

K Number: K970969 · Decision Apr 23, 1997
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
31
Applicant Total
63
Review Days
37

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET
K Number
K970969
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5090
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Kendal Co.
Date Received
March 17, 1997
Decision Date
April 23, 1997
Product Code
KOB
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
KOB Catheter, Suprapubic (And Accessories)

Similar 510(k) Clearances

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

View all

Other Clearances by The Kendal Co.

K Number Device Name
K000087 MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR
K990500 KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946C
K991758 MONOJECT INSULIN SYRINGE
K951488 KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP
K942664 KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM
K942774 POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING
K892434 KENDALL CURITY OXYGEN MASK
K892438 KENDALL CURITY INTRAVASCULAR CUT DOWN TUBES
K892440 KENDALL CURITY EXTENSION TUBES
K892436 KENDALL CURITY IRRIGATION SYRINGE
Search all 63 clearances from The Kendal Co. →