FDA 510(k)

AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS

K-Number: K062850 · 2006-10-23

ApplicantUnited States Surgical, A Division of Tyco Healthc

Decision Date2006-10-23

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 2006-10-23 under 510(k) number K062850. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS?

AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS is a medical device that received FDA 510(k) clearance on 2006-10-23. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K062850.

When did AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS receive FDA 510(k) clearance?

AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS received FDA 510(k) clearance on 2006-10-23, under 510(k) number K062850.

Who is the listed applicant for AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS?

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 CIRCULAR EEA SURGICAL STAPLERS?

The FDA product code for AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS is GDW.

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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.