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FDA 510(k)

TAXO DISCS FOR DIFF. OF ANAEROBES

K-Number: K761209 · 1976-12-09

ApplicantBioquest
Decision Date1976-12-09
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TAXO DISCS FOR DIFF. OF ANAEROBES is the device name listed in this FDA 510(k) record. The listed applicant is Bioquest. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761209. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAXO DISCS FOR DIFF. OF ANAEROBES?

TAXO DISCS FOR DIFF. OF ANAEROBES is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Bioquest. The 510(k) number is K761209.

When did TAXO DISCS FOR DIFF. OF ANAEROBES receive FDA 510(k) clearance?

TAXO DISCS FOR DIFF. OF ANAEROBES received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761209.

Who is the listed applicant for TAXO DISCS FOR DIFF. OF ANAEROBES?

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

What is the FDA product code for TAXO DISCS FOR DIFF. OF ANAEROBES?

The FDA product code for TAXO DISCS FOR DIFF. OF ANAEROBES is JTO.

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Other records listing Bioquest 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.

K760764YEAST ASSIMILATION AGAR

Related Devices (Code: JTO)

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.

K050352IN-VITRO DIAGNOSTIC VAGINITIS TEST KITAmeritek Research, LLCK970832PYR SWABRemel, Inc.K970834GRAM SWABRemel, Inc.K970833INDOLE SWABRemel, Inc.K970009LYFO(TM) DIFFERENTIAL DISK-BACITRACINMicrobiologics, Inc.K962966IDS RAPID CB PLUS SYSTEMInnovative Diagnostic Systems, Inc.

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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