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FDA 510(k)

POWER SUTURE

K-Number: K821702 · 1982-12-15

ApplicantTaylor H. Haynes, M.D.
Decision Date1982-12-15
Product Code
DecisionSubstantially Equivalent

Device Summary

POWER SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Taylor H. Haynes, M.D.. It received FDA 510(k) clearance on 1982-12-15 under 510(k) number K821702. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER SUTURE?

POWER SUTURE is a medical device that received FDA 510(k) clearance on 1982-12-15. The listed applicant is Taylor H. Haynes, M.D.. The 510(k) number is K821702.

When did POWER SUTURE receive FDA 510(k) clearance?

POWER SUTURE received FDA 510(k) clearance on 1982-12-15, under 510(k) number K821702.

Who is the listed applicant for POWER SUTURE?

The FDA 510(k) record lists Taylor H. Haynes, M.D. as the applicant. This does not by itself establish the device manufacturer.

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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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