SURGILENE POLYPROPYLENE SUTURE
K-Number: K930587 · 1993-12-17
Advertisement
Device Summary
Frequently Asked Questions
What is the SURGILENE POLYPROPYLENE SUTURE?
SURGILENE POLYPROPYLENE SUTURE is a medical device that received FDA 510(k) clearance on 1993-12-17. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K930587.
When did SURGILENE POLYPROPYLENE SUTURE receive FDA 510(k) clearance?
SURGILENE POLYPROPYLENE SUTURE received FDA 510(k) clearance on 1993-12-17, under 510(k) number K930587.
Who is the listed applicant for SURGILENE POLYPROPYLENE SUTURE?
The FDA 510(k) record lists Davis & Geck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGILENE POLYPROPYLENE SUTURE?
The FDA product code for SURGILENE POLYPROPYLENE SUTURE is GAW.
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 Davis & Geck, 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: GAW)
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.
Advertisement