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FDA 510(k)

VIRON(TM)

K-Number: K872646 · 1987-09-14

ApplicantbioMerieux, Inc.
Decision Date1987-09-14
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VIRON(TM) is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 1987-09-14 under 510(k) number K872646. The device is classified under product code JJT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIRON(TM)?

VIRON(TM) is a medical device that received FDA 510(k) clearance on 1987-09-14. The listed applicant is bioMerieux, Inc.. The 510(k) number is K872646.

When did VIRON(TM) receive FDA 510(k) clearance?

VIRON(TM) received FDA 510(k) clearance on 1987-09-14, under 510(k) number K872646.

Who is the listed applicant for VIRON(TM)?

The FDA 510(k) record lists bioMerieux, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIRON(TM)?

The FDA product code for VIRON(TM) is JJT.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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