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

TARGET ISOCHECK CONTROL SERUM

K Number: K821183 · Decision May 14, 1982
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
96
Applicant Total
42
Review Days
17

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Basic Information

Device Name
TARGET ISOCHECK CONTROL SERUM
K Number
K821183
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Smithkline Diagnostics, Inc.
Date Received
April 27, 1982
Decision Date
May 14, 1982
Product Code
JJT
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
JJT Enzyme Controls (Assayed And Unassayed)

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K934863 FLEXSURE HP
K880499 HEMOCCULT SENSITIVE TEST
K875131 (SKD) CHOLESTEROL TEST KIT
K862849 HEMOCCULT WIPE TEST
K854723 SKD ELECTROCHEMICAL SYSTEM (ECS)
K852841 RAPID DIRECT STREP A LATEX AGGLUTINATION TEST
K821884 GASTROCCULT TM
K821674 SPINCHEM ACID PHOSPHATASE REAGENT
Search all 42 clearances from Smithkline Diagnostics, Inc. →