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FDA 510(k)

VITEK YEAST BIOCHEMICAL CARD

K-Number: K881925 · 1988-06-16

Decision Date1988-06-16
Product CodeJXB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VITEK YEAST BIOCHEMICAL CARD is the device name listed in this FDA 510(k) record. The listed applicant is Vitek Systems, Inc.. It received FDA 510(k) clearance on 1988-06-16 under 510(k) number K881925. The device is classified under product code JXB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITEK YEAST BIOCHEMICAL CARD?

VITEK YEAST BIOCHEMICAL CARD is a medical device that received FDA 510(k) clearance on 1988-06-16. The listed applicant is Vitek Systems, Inc.. The 510(k) number is K881925.

When did VITEK YEAST BIOCHEMICAL CARD receive FDA 510(k) clearance?

VITEK YEAST BIOCHEMICAL CARD received FDA 510(k) clearance on 1988-06-16, under 510(k) number K881925.

Who is the listed applicant for VITEK YEAST BIOCHEMICAL CARD?

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

What is the FDA product code for VITEK YEAST BIOCHEMICAL CARD?

The FDA product code for VITEK YEAST BIOCHEMICAL CARD is JXB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Vitek Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 39 devices →

Related Devices (Code: JXB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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