3M Ige Single Point Fast Test

FDA 510(k) K913212 · Whittaker Bioproducts, Inc.

Substantially Equivalent

510(k) numberK913212

Submission

Device name
3M Ige Single Point Fast Test
Applicant
Whittaker Bioproducts, Inc.
Walkersville, MD, US
Received
July 19, 1991
Decision date
November 22, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DHB – System, Test, Radioallergosorbent (Rast) Immunological
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5750
Specialty
Immunology

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Questions and answers

When was 3M Ige Single Point Fast Test cleared by the FDA?

3M Ige Single Point Fast Test (K913212) received a 510(k) decision of Substantially Equivalent on November 22, 1991, 126 days after the submission was received.

What is the product code of K913212?

The FDA product code is DHB – System, Test, Radioallergosorbent (Rast) Immunological, a Class II (moderate risk) device regulated under 21 CFR 866.5750.