Spinchem Acid Phosphatase Reagent

FDA 510(k) K821674 · Smithkline Diagnostics, Inc.

Substantially Equivalent

510(k) numberK821674

Submission

Device name
Spinchem Acid Phosphatase Reagent
Applicant
Smithkline Diagnostics, Inc.
Mchenry, IL, US
Received
June 7, 1982
Decision date
June 22, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CKB – Acid Phosphatase, Naphthyl Phosphate
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1020
Specialty
Clinical Chemistry

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K902495Acid Phosphatase Reagent SetCKB · Traditional Tech Intl. Co.07/16/1990SE
K892393Acid Phosphatase ReagentCKB · Traditional Medical Analysis Systems, Inc.07/20/1989SE

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Questions and answers

When was Spinchem Acid Phosphatase Reagent cleared by the FDA?

Spinchem Acid Phosphatase Reagent (K821674) received a 510(k) decision of Substantially Equivalent on June 22, 1982, 15 days after the submission was received.

What is the product code of K821674?

The FDA product code is CKB – Acid Phosphatase, Naphthyl Phosphate, a Class II (moderate risk) device regulated under 21 CFR 862.1020.