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FDA 510(k)

RAPID NFT, MODIFICATION

K-Number: K922768 · 1992-10-14

ApplicantBiomerieux Vitek, Inc.
Decision Date1992-10-14
Product CodeJSW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

RAPID NFT, MODIFICATION 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 1992-10-14 under 510(k) number K922768. The device is classified under product code JSW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAPID NFT, MODIFICATION?

RAPID NFT, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-10-14. The listed applicant is Biomerieux Vitek, Inc.. The 510(k) number is K922768.

When did RAPID NFT, MODIFICATION receive FDA 510(k) clearance?

RAPID NFT, MODIFICATION received FDA 510(k) clearance on 1992-10-14, under 510(k) number K922768.

Who is the listed applicant for RAPID NFT, MODIFICATION?

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 RAPID NFT, MODIFICATION?

The FDA product code for RAPID NFT, MODIFICATION is JSW.

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Other records listing Biomerieux Vitek, Inc. as applicant

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Related Devices (Code: JSW)

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.

K900517RAPID NF SYSTEMInnovative Diagnostic Systems, Inc.K870769AUSTIN NONFERMENTER KITAustin Biological LaboratoriesK790992PSEUDO-PALETTE TMMicro-Palettes, Inc.K772112NON-FERMENTER SYSTEMCorning Medical & ScientificK770745PANEL, GNF, MICRO-IDMicro-Media Systems, Inc.

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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