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FDA 510(k)

ADVANCE SUTURE NONABSORBABLE DACRON SUTURE

K-Number: K903175 · 1991-07-26

Decision Date1991-07-26
Product CodeGAS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADVANCE SUTURE NONABSORBABLE DACRON SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Advance Suture, Inc.. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K903175. The device is classified under product code GAS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCE SUTURE NONABSORBABLE DACRON SUTURE?

ADVANCE SUTURE NONABSORBABLE DACRON SUTURE is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Advance Suture, Inc.. The 510(k) number is K903175.

When did ADVANCE SUTURE NONABSORBABLE DACRON SUTURE receive FDA 510(k) clearance?

ADVANCE SUTURE NONABSORBABLE DACRON SUTURE received FDA 510(k) clearance on 1991-07-26, under 510(k) number K903175.

Who is the listed applicant for ADVANCE SUTURE NONABSORBABLE DACRON SUTURE?

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

What is the FDA product code for ADVANCE SUTURE NONABSORBABLE DACRON SUTURE?

The FDA product code for ADVANCE SUTURE NONABSORBABLE DACRON SUTURE is GAS.

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 Advance Suture, 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.

Related Devices (Code: GAS)

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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