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

OLYMPUS GUIDE WIRE

K Number: K933110 · Decision Nov 4, 1993
Classifications
1
FEI Numbers
91
Registration Numbers
91
Same Product Code
42
Applicant Total
142
Review Days
132

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Basic Information

Device Name
OLYMPUS GUIDE WIRE
K Number
K933110
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Olympus Corp.
Date Received
June 25, 1993
Decision Date
November 4, 1993
Product Code
OCY
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
OCY Endoscopic Guidewire, Gastroenterology-Urology

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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. →