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

SERUM IRON

K Number: K771838 · Decision Nov 3, 1977
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
66
Applicant Total
23
Review Days
43

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Basic Information

Device Name
SERUM IRON
K Number
K771838
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1410
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Gamma Enterprises, Inc.
Date Received
September 21, 1977
Decision Date
November 3, 1977
Product Code
JIY
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
JIY Photometric Method, Iron (Non-Heme)

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Other Clearances by Gamma Enterprises, Inc.

K Number Device Name
K790578 GAMMA SMAC REAGENTS
K780507 SERUM GLUTAMIC-PYRUVIC TRANSAMINASE
K780505 SERUM GLUTAMIC-OXALOACETIC-TRANSAMINASE
K780504 CREATINE PHOSPHOKINASE (CPK)
K780506 CARBON DIOXIDE REAGENTS
K771843 WETTING AGENTS
K771832 CHLORIDE
K771836 LACTATE DEHYDROGENASE
K771834 CREATININE
K771829 ALKALINE PHOSPHATASE
Search all 23 clearances from Gamma Enterprises, Inc. →