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FDA 510(k)

WINGMASTER

K-Number: K921355 · 1992-09-25

Decision Date1992-09-25
Product CodeEHB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WINGMASTER is the device name listed in this FDA 510(k) record. The listed applicant is Innovators, Inc.. It received FDA 510(k) clearance on 1992-09-25 under 510(k) number K921355. The device is classified under product code EHB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WINGMASTER?

WINGMASTER is a medical device that received FDA 510(k) clearance on 1992-09-25. The listed applicant is Innovators, Inc.. The 510(k) number is K921355.

When did WINGMASTER receive FDA 510(k) clearance?

WINGMASTER received FDA 510(k) clearance on 1992-09-25, under 510(k) number K921355.

Who is the listed applicant for WINGMASTER?

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

What is the FDA product code for WINGMASTER?

The FDA product code for WINGMASTER is EHB.

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 Innovators, 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.

Related Devices (Code: EHB)

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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