Immuchem Covalent Coat Solid Phase Assay

FDA 510(k) K791663 · Immuchem Corp.

Substantially Equivalent

510(k) numberK791663

Submission

Device name
Immuchem Covalent Coat Solid Phase Assay
Applicant
Immuchem Corp.
Mchenry, IL, US
Received
August 21, 1979
Decision date
October 1, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CDP – Radioimmunoassay, Total Triiodothyronine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1710
Specialty
Clinical Chemistry

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Questions and answers

When was Immuchem Covalent Coat Solid Phase Assay cleared by the FDA?

Immuchem Covalent Coat Solid Phase Assay (K791663) received a 510(k) decision of Substantially Equivalent on October 1, 1979, 41 days after the submission was received.

What is the product code of K791663?

The FDA product code is CDP – Radioimmunoassay, Total Triiodothyronine, a Class II (moderate risk) device regulated under 21 CFR 862.1710.