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FDA 510(k)

DEROYAL SURGICAL INSTRUMENT DRAPE

K-Number: K950565 · 1995-12-13

Decision Date1995-12-13
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEROYAL SURGICAL INSTRUMENT DRAPE 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 1995-12-13 under 510(k) number K950565. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEROYAL SURGICAL INSTRUMENT DRAPE?

DEROYAL SURGICAL INSTRUMENT DRAPE is a medical device that received FDA 510(k) clearance on 1995-12-13. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K950565.

When did DEROYAL SURGICAL INSTRUMENT DRAPE receive FDA 510(k) clearance?

DEROYAL SURGICAL INSTRUMENT DRAPE received FDA 510(k) clearance on 1995-12-13, under 510(k) number K950565.

Who is the listed applicant for DEROYAL SURGICAL INSTRUMENT DRAPE?

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 SURGICAL INSTRUMENT DRAPE?

The FDA product code for DEROYAL SURGICAL INSTRUMENT DRAPE is KKX.

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: KKX)

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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