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FDA 510(k)

LUKENS SILK SURGICAL SUTURE

K-Number: K930942 · 1993-12-17

Decision Date1993-12-17
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LUKENS SILK SURGICAL SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Lukens Medical Corp.. It received FDA 510(k) clearance on 1993-12-17 under 510(k) number K930942. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUKENS SILK SURGICAL SUTURE?

LUKENS SILK SURGICAL SUTURE is a medical device that received FDA 510(k) clearance on 1993-12-17. The listed applicant is Lukens Medical Corp.. The 510(k) number is K930942.

When did LUKENS SILK SURGICAL SUTURE receive FDA 510(k) clearance?

LUKENS SILK SURGICAL SUTURE received FDA 510(k) clearance on 1993-12-17, under 510(k) number K930942.

Who is the listed applicant for LUKENS SILK SURGICAL SUTURE?

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

What is the FDA product code for LUKENS SILK SURGICAL SUTURE?

The FDA product code for LUKENS SILK SURGICAL SUTURE is GAT.

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 Lukens Medical Corp. 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 8 devices →

Related Devices (Code: GAT)

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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