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FDA 510(k)

DEROYAL TRANSPARENT FILM DRESSIGN

K-Number: K920796 · 1992-07-23

Decision Date1992-07-23
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

DEROYAL TRANSPARENT FILM DRESSIGN is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 1992-07-23 under 510(k) number K920796. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEROYAL TRANSPARENT FILM DRESSIGN?

DEROYAL TRANSPARENT FILM DRESSIGN is a medical device that received FDA 510(k) clearance on 1992-07-23. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K920796.

When did DEROYAL TRANSPARENT FILM DRESSIGN receive FDA 510(k) clearance?

DEROYAL TRANSPARENT FILM DRESSIGN received FDA 510(k) clearance on 1992-07-23, under 510(k) number K920796.

Who is the listed applicant for DEROYAL TRANSPARENT FILM DRESSIGN?

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

What is the FDA product code for DEROYAL TRANSPARENT FILM DRESSIGN?

The FDA product code for DEROYAL TRANSPARENT FILM DRESSIGN is MGP.

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 Deroyal Industries, 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.

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Related Devices (Code: MGP)

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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