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

LOWSLEY SUPRAPUBIC TRACTOR

K Number: K012153 · Decision Sep 19, 2001
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
31
Applicant Total
14
Review Days
70

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Basic Information

Device Name
LOWSLEY SUPRAPUBIC TRACTOR
K Number
K012153
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5090
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Circon Video
Date Received
July 11, 2001
Decision Date
September 19, 2001
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.

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Other Clearances by Circon Video

K Number Device Name
K012758 URETEROSCOPE, PEDIATRIC CYSTOURETEROSCOPE, OPERATING PEDIATRIC CYSTOURETEROSCOPE, MODELS MR-9, MR-9L,
K011876 DOLPHIN II FLUID MANAGEMENT SYSTEM, MODEL DOL-2
K011849 MICRO-6-SERIES (MR-6, MR-6L) URETEROSCOPES, MRO-6 SERIES (MR-633, MR-642) URETEROSCOPES, MRO-7 SERIES (MRO-733) URETEROS
K012929 FLEXIBLE PEDIATRIC CYSTOURETEROSCOPE, MODEL AUR- 735
K012951 APN-2 USA SERIES FLEXIBLE CHOLEDOCHOSCOPE
K012925 DUR-8, MODELS DUR-8
K012265 METAL HALIDE LIGHT SOURCE, MODELS MV-9088-T, MV-9088
K011848 CIRCON AEH-4 ELECTROHYDRAULIC LITHOTRIPSY PROBE
K970595 CIRCON ENDOTEK OM-4 H2O CYSTOMETRY PUMP
K914883 CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG
Search all 14 clearances from Circon Video →