GIA™ Stapler with Tri-Staple™ Technology
K-Number: K231934 · 2023-10-27
Device Summary
Frequently Asked Questions
What is the GIA™ Stapler with Tri-Staple™ Technology?
GIA™ Stapler with Tri-Staple™ Technology is a medical device that received FDA 510(k) clearance on 2023-10-27. The listed applicant is Covidien. The 510(k) number is K231934.
When did GIA™ Stapler with Tri-Staple™ Technology receive FDA 510(k) clearance?
GIA™ Stapler with Tri-Staple™ Technology received FDA 510(k) clearance on 2023-10-27, under 510(k) number K231934.
Who is the listed applicant for GIA™ Stapler with Tri-Staple™ Technology?
The FDA 510(k) record lists Covidien as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GIA™ Stapler with Tri-Staple™ Technology?
The FDA product code for GIA™ Stapler with Tri-Staple™ Technology is GAG.
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 Covidien 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: GAG)
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.