Icon Strep B Immunoenzymetric Assay

FDA 510(k) K902991 · Hybritech, Inc.

Substantially Equivalent

510(k) numberK902991

Submission

Device name
Icon Strep B Immunoenzymetric Assay
Applicant
Hybritech, Inc.
San Diego, CA, US
Received
July 9, 1990
Decision date
October 3, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GTY – Antigens, All Groups, Streptococcus Spp.
Device class
Class I (low risk)
Regulation
21 CFR 866.3740
Specialty
Microbiology

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K922754Tandem-E Ige II Calibration Verification SetJJX · Traditional 02/17/1993SE
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K920556Tandem-E HCG Calibration Verification Control SetJJX · Traditional 07/17/1992SE
K921763Tandem Icon QSR CKMB Immunoenzymetric AssayJHY · Traditional 06/09/1992SE
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K911417Icon Strep B Immunoenzymetric AssayGTZ · Traditional 07/24/1991SE

Questions and answers

When was Icon Strep B Immunoenzymetric Assay cleared by the FDA?

Icon Strep B Immunoenzymetric Assay (K902991) received a 510(k) decision of Substantially Equivalent on October 3, 1990, 86 days after the submission was received.

What is the product code of K902991?

The FDA product code is GTY – Antigens, All Groups, Streptococcus Spp., a Class I (low risk) device regulated under 21 CFR 866.3740.