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FDA 510(k)

MICROTEK MEDICAL'S SOUND STIKS

K-Number: K913276 · 1991-10-21

Decision Date1991-10-21
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MICROTEK MEDICAL'S SOUND STIKS is the device name listed in this FDA 510(k) record. The listed applicant is Microbio-Medics, Inc.. It received FDA 510(k) clearance on 1991-10-21 under 510(k) number K913276. The device is classified under product code EWO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROTEK MEDICAL'S SOUND STIKS?

MICROTEK MEDICAL'S SOUND STIKS is a medical device that received FDA 510(k) clearance on 1991-10-21. The listed applicant is Microbio-Medics, Inc.. The 510(k) number is K913276.

When did MICROTEK MEDICAL'S SOUND STIKS receive FDA 510(k) clearance?

MICROTEK MEDICAL'S SOUND STIKS received FDA 510(k) clearance on 1991-10-21, under 510(k) number K913276.

Who is the listed applicant for MICROTEK MEDICAL'S SOUND STIKS?

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

What is the FDA product code for MICROTEK MEDICAL'S SOUND STIKS?

The FDA product code for MICROTEK MEDICAL'S SOUND STIKS is EWO.

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 Microbio-Medics, 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 13 devices →

Related Devices (Code: EWO)

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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