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FDA 510(k)

FAS FASTIDIOUS MIC PANEL

K-Number: K935485 · 1995-02-16

Decision Date1995-02-16
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

FAS FASTIDIOUS MIC PANEL is the device name listed in this FDA 510(k) record. The listed applicant is Microtech Medical Systems, Inc.. It received FDA 510(k) clearance on 1995-02-16 under 510(k) number K935485. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FAS FASTIDIOUS MIC PANEL?

FAS FASTIDIOUS MIC PANEL is a medical device that received FDA 510(k) clearance on 1995-02-16. The listed applicant is Microtech Medical Systems, Inc.. The 510(k) number is K935485.

When did FAS FASTIDIOUS MIC PANEL receive FDA 510(k) clearance?

FAS FASTIDIOUS MIC PANEL received FDA 510(k) clearance on 1995-02-16, under 510(k) number K935485.

Who is the listed applicant for FAS FASTIDIOUS MIC PANEL?

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

What is the FDA product code for FAS FASTIDIOUS MIC PANEL?

The FDA product code for FAS FASTIDIOUS MIC PANEL is JWY.

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 Microtech Medical 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 12 devices →

Related Devices (Code: JWY)

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

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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