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

ALKALINE PHOSPHATASE-RATE

K Number: K833744 · Decision Jan 13, 1984
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
123
Applicant Total
20
Review Days
79

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Basic Information

Device Name
ALKALINE PHOSPHATASE-RATE
K Number
K833744
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Seragen Diagnostics, Inc.
Date Received
October 26, 1983
Decision Date
January 13, 1984
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

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Other Clearances by Seragen Diagnostics, Inc.

K Number Device Name
K872148 VIVID CHLAMYDIA(TM)
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K852260 QUICK-CHEM CALIBRATION SET
K851520 CK/LD ISOENZYMES CONTROLS(HUMAN)
K851521 LD-1(IMMUNO) SEPARATION SET
K850209 QUICK-LYTE
K844743 SERATEST ENA(RNP/SM) DETERMINATION
K842563 SERATEST DNA DETERMINATION
K841504 QUICK-COUNT PLUS 2
K840793 CK/MB IMMUNO-ISOENZYME CONTROL SERUM
Search all 20 clearances from Seragen Diagnostics, Inc. →