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

OLYMPUS OES LAPAROSCOPY SYSTEM

K Number: K923982 · Decision Mar 15, 1993
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
142
Review Days
220

Basic Information

Device Name
OLYMPUS OES LAPAROSCOPY SYSTEM
K Number
K923982
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
OLYMPUS CORP.
Date Received
August 7, 1992
Decision Date
March 15, 1993
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

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Other Clearances by OLYMPUS CORP.

K Number Device Name
K915402 EW-10 AND EW-20
K933200 OLYMPUS PBD STENTS
K942338 OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIES
K931763 HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESS
K934835 FLOVAL
K931764 HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES
K915857 FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE
K931994 RESECTOSCOPE SHEATH
K933992 OLYMPUS SCLEROTHERAPY BALLOON
K934361 OLYMPUS CREATININE REAGENT
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