Enzymun Test R Ige

FDA 510(k) K896902 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK896902

Submission

Device name
Enzymun Test R Ige
Applicant
Boehringer Mannheim Corp.
Indianapolis, IN, US
Received
December 8, 1989
Decision date
January 10, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Enzymun Test R Ige cleared by the FDA?

Enzymun Test R Ige (K896902) received a 510(k) decision of Substantially Equivalent on January 10, 1990, 33 days after the submission was received.

What is the product code of K896902?

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