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

ALKALINE PHOSPHATASE, THYMOLPHTHALEIN MONOPHOSPHAT

K Number: K880177 · Decision Apr 5, 1988
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
10
Applicant Total
36
Review Days
81

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Basic Information

Device Name
ALKALINE PHOSPHATASE, THYMOLPHTHALEIN MONOPHOSPHAT
K Number
K880177
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Tech-Co, Inc.
Date Received
January 15, 1988
Decision Date
April 5, 1988
Product Code
CIO
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
CIO Thymolphthalein Monophosphate, Alkaline Phosphatase Or Isoenzymes

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Other Clearances by Tech-Co, Inc.

K Number Device Name
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K923376 VISUAL HCG PREGNANCY TEST
K920766 T4 EIA BEAD ASSAY
K920716 DIRECT PREGNANCY TEST
K902574 POTASSIUM REAGENT SET
K901561 IRON/TOTAL IRON BINDING CAPACITY
K883387 ALANINE AMINO TRANSFERASE (COLORIMETRIC METHOD)
K883683 HEMOGLOBIN
K883386 CHLORIDE
K881172 BILIRUBIN (DIRECT)
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