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FDA 510(k)

PANEL, GNF, MICRO-ID

K-Number: K770745 · 1977-06-23

ApplicantMicro-Media Systems, Inc.
Decision Date1977-06-23
Product CodeJSW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PANEL, GNF, MICRO-ID is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Media Systems, Inc.. It received FDA 510(k) clearance on 1977-06-23 under 510(k) number K770745. 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 PANEL, GNF, MICRO-ID?

PANEL, GNF, MICRO-ID is a medical device that received FDA 510(k) clearance on 1977-06-23. The listed applicant is Micro-Media Systems, Inc.. The 510(k) number is K770745.

When did PANEL, GNF, MICRO-ID receive FDA 510(k) clearance?

PANEL, GNF, MICRO-ID received FDA 510(k) clearance on 1977-06-23, under 510(k) number K770745.

Who is the listed applicant for PANEL, GNF, MICRO-ID?

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

What is the FDA product code for PANEL, GNF, MICRO-ID?

The FDA product code for PANEL, GNF, MICRO-ID is JSW.

Related Clinical Trials

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Other records listing Micro-Media 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.

K953422FOX FASTIDIOUS TEST PANELSK945997MODIFIED FOX EXTRA GRAM POSITIVEK823738GRAM NEGATIVE BACTERIAL IDENTIF- PANELSK801547TEST PANEL FOR PRESUMP. ID/BACT. ORGK791991STREP-SPECK770746PANEL, IDENTIFICATION, STREP, MICRO-ID

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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.

K922768RAPID NFT, MODIFICATIONBiomerieux Vitek, Inc.K900517RAPID NF SYSTEMInnovative Diagnostic Systems, Inc.K870769AUSTIN NONFERMENTER KITAustin Biological LaboratoriesK790992PSEUDO-PALETTE TMMicro-Palettes, Inc.K772112NON-FERMENTER SYSTEMCorning Medical & Scientific

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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