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FDA 510(k)

STERAID SURGICAL DRESSING

K-Number: K790631 · 1979-07-30

Decision Date1979-07-30
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

STERAID SURGICAL DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Corda Intl. Holdings, Inc.. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K790631. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERAID SURGICAL DRESSING?

STERAID SURGICAL DRESSING is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Corda Intl. Holdings, Inc.. The 510(k) number is K790631.

When did STERAID SURGICAL DRESSING receive FDA 510(k) clearance?

STERAID SURGICAL DRESSING received FDA 510(k) clearance on 1979-07-30, under 510(k) number K790631.

Who is the listed applicant for STERAID SURGICAL DRESSING?

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

What is the FDA product code for STERAID SURGICAL DRESSING?

The FDA product code for STERAID SURGICAL DRESSING is EFQ.

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.

Related Devices (Code: EFQ)

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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