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FDA 510(k)

MINIVIDAS INSTRUMENT

K-Number: K923579 · 1993-02-12

ApplicantBiomerieux Vitek, Inc.
Decision Date1993-02-12
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MINIVIDAS INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Biomerieux Vitek, Inc.. It received FDA 510(k) clearance on 1993-02-12 under 510(k) number K923579. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIVIDAS INSTRUMENT?

MINIVIDAS INSTRUMENT is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Biomerieux Vitek, Inc.. The 510(k) number is K923579.

When did MINIVIDAS INSTRUMENT receive FDA 510(k) clearance?

MINIVIDAS INSTRUMENT received FDA 510(k) clearance on 1993-02-12, under 510(k) number K923579.

Who is the listed applicant for MINIVIDAS INSTRUMENT?

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

What is the FDA product code for MINIVIDAS INSTRUMENT?

The FDA product code for MINIVIDAS INSTRUMENT is JJE.

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Other records listing Biomerieux Vitek, Inc. as applicant

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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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