Respirastick Enzyme Immunoassay Test

FDA 510(k) K862475 · Orion Diagnostica, Inc.

Substantially Equivalent

510(k) numberK862475

Submission

Device name
Respirastick Enzyme Immunoassay Test
Applicant
Orion Diagnostica, Inc.
Somerset, NJ, US
Received
June 30, 1986
Decision date
September 16, 1986
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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Questions and answers

When was Respirastick Enzyme Immunoassay Test cleared by the FDA?

Respirastick Enzyme Immunoassay Test (K862475) received a 510(k) decision of Substantially Equivalent on September 16, 1986, 78 days after the submission was received.

What is the product code of K862475?

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