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

OLYMPUS RIGID PERCUTANEOUS NEPHROSCOPE

K Number: K853486 · Decision Sep 12, 1985
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
9
Applicant Total
142
Review Days
23

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Basic Information

Device Name
OLYMPUS RIGID PERCUTANEOUS NEPHROSCOPE
K Number
K853486
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Olympus Corp.
Date Received
August 20, 1985
Decision Date
September 12, 1985
Product Code
FGA
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
FGA Kit, Nephroscope

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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
Search all 142 clearances from Olympus Corp. →