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FDA 510(k)

ANAEROBIC MIC PANEL

K-Number: K884831 · 1989-03-27

Decision Date1989-03-27
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANAEROBIC 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 1989-03-27 under 510(k) number K884831. 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 ANAEROBIC MIC PANEL?

ANAEROBIC MIC PANEL is a medical device that received FDA 510(k) clearance on 1989-03-27. The listed applicant is Microtech Medical Systems, Inc.. The 510(k) number is K884831.

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

ANAEROBIC MIC PANEL received FDA 510(k) clearance on 1989-03-27, under 510(k) number K884831.

Who is the listed applicant for ANAEROBIC 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 ANAEROBIC MIC PANEL?

The FDA product code for ANAEROBIC 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

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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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