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

OLYMPUS CREATININE REAGENT

K Number: K931939 · Decision Sep 21, 1993
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
158
Applicant Total
142
Review Days
155

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Basic Information

Device Name
OLYMPUS CREATININE REAGENT
K Number
K931939
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1225
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Olympus Corp.
Date Received
April 19, 1993
Decision Date
September 21, 1993
Product Code
CGX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CGX Alkaline Picrate, Colorimetry, Creatinine

Similar 510(k) Clearances

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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. →