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FDA 510(k)

L-25 ABSORBABLE SURIGCAL SUTURE

K-Number: K013671 · 2002-01-08

Decision Date2002-01-08
Product CodeGAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

L-25 ABSORBABLE SURIGCAL SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 2002-01-08 under 510(k) number K013671. The device is classified under product code GAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L-25 ABSORBABLE SURIGCAL SUTURE?

L-25 ABSORBABLE SURIGCAL SUTURE is a medical device that received FDA 510(k) clearance on 2002-01-08. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K013671.

When did L-25 ABSORBABLE SURIGCAL SUTURE receive FDA 510(k) clearance?

L-25 ABSORBABLE SURIGCAL SUTURE received FDA 510(k) clearance on 2002-01-08, under 510(k) number K013671.

Who is the listed applicant for L-25 ABSORBABLE SURIGCAL SUTURE?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L-25 ABSORBABLE SURIGCAL SUTURE?

The FDA product code for L-25 ABSORBABLE SURIGCAL SUTURE is GAM.

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 United States Surgical, A Division of Tyco Healthc 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.

View all 218 devices →

Related Devices (Code: GAM)

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

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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