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FDA 510(k)

SURGICAL RETRACTOR & ELASTIC STAYS, DISP

K-Number: K812562 · 1981-10-02

Decision Date1981-10-02
Product CodeGDG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL RETRACTOR & ELASTIC STAYS, DISP is the device name listed in this FDA 510(k) record. The listed applicant is Humboldt Products. It received FDA 510(k) clearance on 1981-10-02 under 510(k) number K812562. The device is classified under product code GDG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL RETRACTOR & ELASTIC STAYS, DISP?

SURGICAL RETRACTOR & ELASTIC STAYS, DISP is a medical device that received FDA 510(k) clearance on 1981-10-02. The listed applicant is Humboldt Products. The 510(k) number is K812562.

When did SURGICAL RETRACTOR & ELASTIC STAYS, DISP receive FDA 510(k) clearance?

SURGICAL RETRACTOR & ELASTIC STAYS, DISP received FDA 510(k) clearance on 1981-10-02, under 510(k) number K812562.

Who is the listed applicant for SURGICAL RETRACTOR & ELASTIC STAYS, DISP?

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

What is the FDA product code for SURGICAL RETRACTOR & ELASTIC STAYS, DISP?

The FDA product code for SURGICAL RETRACTOR & ELASTIC STAYS, DISP is GDG.

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 Humboldt Products 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: GDG)

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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