FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OLYMPUS INORGANIC PHOSPHORUS REAGENT

K Number: K923564 · Decision Aug 18, 1992
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
142
Review Days
32

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Basic Information

Device Name
OLYMPUS INORGANIC PHOSPHORUS REAGENT
K Number
K923564
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Olympus Corp.
Date Received
July 17, 1992
Decision Date
August 18, 1992
Product Code
CEO
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
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus

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. →