FDA 510(k)

AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE

K-Number: K934720 · 1994-03-25

ApplicantUnited States Surgical, A Division of Tyco Healthc

Decision Date1994-03-25

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE 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 1994-03-25 under 510(k) number K934720. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE?

AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE is a medical device that received FDA 510(k) clearance on 1994-03-25. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K934720.

When did AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE receive FDA 510(k) clearance?

AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE received FDA 510(k) clearance on 1994-03-25, under 510(k) number K934720.

Who is the listed applicant for AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE?

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 AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE?

The FDA product code for AUTO SUTURE DISPOSABLE ARTHROSCOPIC TROCAR AND SLEEVE is HRX.

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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.