AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIER
K-Number: K071406 · 2007-11-21
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Device Summary
Frequently Asked Questions
What is the AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIER?
AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIER is a medical device that received FDA 510(k) clearance on 2007-11-21. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K071406.
When did AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIER receive FDA 510(k) clearance?
AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIER received FDA 510(k) clearance on 2007-11-21, under 510(k) number K071406.
Who is the listed applicant for AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIER?
The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIER?
The FDA product code for AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIER is FZP.
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 United States Surgical, A Division of Tyco Healthc 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: FZP)
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.
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