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

ALKALINE PHOSPHATASE

K Number: K771829 · Decision Nov 2, 1977
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
122
Applicant Total
23
Review Days
42

Basic Information

Device Name
ALKALINE PHOSPHATASE
K Number
K771829
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
GAMMA ENTERPRISES, INC.
Date Received
September 21, 1977
Decision Date
November 2, 1977
Product Code
CJE
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
CJE Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CJE), ordered by most recent decision date.

View all

Other Clearances by GAMMA ENTERPRISES, INC.

K Number Device Name
K790578 GAMMA SMAC REAGENTS
K780504 CREATINE PHOSPHOKINASE (CPK)
K780507 SERUM GLUTAMIC-PYRUVIC TRANSAMINASE
K780505 SERUM GLUTAMIC-OXALOACETIC-TRANSAMINASE
K780506 CARBON DIOXIDE REAGENTS
K771836 LACTATE DEHYDROGENASE
K771832 CHLORIDE
K771843 WETTING AGENTS
K771834 CREATININE
K771838 SERUM IRON
Search all 23 clearances from GAMMA ENTERPRISES, INC. →