Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture
K-Number: K151165 · 2016-02-17
Device Summary
Frequently Asked Questions
What is the Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture?
Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture is a medical device that received FDA 510(k) clearance on 2016-02-17. It is manufactured by Aesculap, Inc.. The 510(k) number is K151165.
When was Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture approved by the FDA?
Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture received FDA 510(k) clearance on 2016-02-17, under approval number K151165.
What company makes Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture?
Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture is manufactured by Aesculap, Inc..
What is the FDA product code for Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture?
The FDA product code for Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture is GAR.
Related Clinical Trials
Other Devices by Aesculap, Inc.
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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.