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

IMMUCHEM COVALENT COAT SOLID PHASE ASSAY

K Number: K791663 · Decision Oct 1, 1979
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
143
Applicant Total
18
Review Days
41

Basic Information

Device Name
IMMUCHEM COVALENT COAT SOLID PHASE ASSAY
K Number
K791663
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
IMMUCHEM CORP.
Date Received
August 21, 1979
Decision Date
October 1, 1979
Product Code
CDP
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
CDP Radioimmunoassay, Total Triiodothyronine

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Other Clearances by IMMUCHEM CORP.

K Number Device Name
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K871542 HPROLACTIN KIT
K865071 THYROID STIMULATING HORMONE (TSH IRMA) RIA KIT
K864144 LUTEINIZING HORMONE (LH-IRMA) RIA KIT
K860559 ANDROSTENEDIONE 125I KIT BY RIA
K854094 IMMUCHEM COVALENT COAT A SOLID PHASE RADIOIMMUNOAS
K830962 IMMUCHEM COVALENT-COAT RIA KIT
K822509 COVALENT COAT RIA KIT
K822140 IMMUCHEM COVALENT-COAT
Search all 18 clearances from IMMUCHEM CORP. →