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. The listed applicant is Aesculap, Inc.. The 510(k) number is K151165.
When did Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture receive FDA 510(k) clearance?
Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture received FDA 510(k) clearance on 2016-02-17, under 510(k) number K151165.
Who is the listed applicant for Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture?
The FDA 510(k) record lists Aesculap, Inc. as the applicant. This does not by itself establish the device manufacturer.
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
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 Aesculap, 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: GAR)
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.