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FDA 510(k)

MICROCLIP, WILLIAMS

K-Number: K780586 · 1978-05-16

Decision Date1978-05-16
Product CodeGDW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROCLIP, WILLIAMS is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1978-05-16 under 510(k) number K780586. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROCLIP, WILLIAMS?

MICROCLIP, WILLIAMS is a medical device that received FDA 510(k) clearance on 1978-05-16. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K780586.

When did MICROCLIP, WILLIAMS receive FDA 510(k) clearance?

MICROCLIP, WILLIAMS received FDA 510(k) clearance on 1978-05-16, under 510(k) number K780586.

Who is the listed applicant for MICROCLIP, WILLIAMS?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROCLIP, WILLIAMS?

The FDA product code for MICROCLIP, WILLIAMS is GDW.

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 Richard'S Medical Equip., 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: GDW)

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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Official Source

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