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

ADULT RESECTOSCOPE

K Number: K890328 · Decision Feb 6, 1990
Classifications
1
FEI Numbers
135
Registration Numbers
135
Same Product Code
170
Applicant Total
14
Review Days
379

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Basic Information

Device Name
ADULT RESECTOSCOPE
K Number
K890328
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1690
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Circon Video
Date Received
January 23, 1989
Decision Date
February 6, 1990
Product Code
HIH
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
HIH Hysteroscope (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HIH), 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 →