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

CIRCON ACMI CAT.# LAP 9900; HIGH FLOW INSUFFLATOR

K Number: K914101 · Decision Nov 22, 1991
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
176
Applicant Total
14
Review Days
71

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Basic Information

Device Name
CIRCON ACMI CAT.# LAP 9900; HIGH FLOW INSUFFLATOR
K Number
K914101
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1730
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Circon Video
Date Received
September 12, 1991
Decision Date
November 22, 1991
Product Code
HIF
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HIF Insufflator, Laparoscopic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HIF), 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
K012153 LOWSLEY SUPRAPUBIC TRACTOR
K011848 CIRCON AEH-4 ELECTROHYDRAULIC LITHOTRIPSY PROBE
K970595 CIRCON ENDOTEK OM-4 H2O CYSTOMETRY PUMP
Search all 14 clearances from Circon Video →