Aesculap Slim Clip Applier Forceps
K-Number: K173271 · 2017-11-10
Device Summary
Frequently Asked Questions
What is the Aesculap Slim Clip Applier Forceps?
Aesculap Slim Clip Applier Forceps is a medical device that received FDA 510(k) clearance on 2017-11-10. The listed applicant is Aesculap, Inc.. The 510(k) number is K173271.
When did Aesculap Slim Clip Applier Forceps receive FDA 510(k) clearance?
Aesculap Slim Clip Applier Forceps received FDA 510(k) clearance on 2017-11-10, under 510(k) number K173271.
Who is the listed applicant for Aesculap Slim Clip Applier Forceps?
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 Slim Clip Applier Forceps?
The FDA product code for Aesculap Slim Clip Applier Forceps is HCI.
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: HCI)
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.