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FDA 510(k)

AUTO SUTURE LAPAROSCOPY ACCESSORY KIT

K-Number: K903780 · 1990-10-23

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1990-10-23
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE LAPAROSCOPY ACCESSORY KIT 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 1990-10-23 under 510(k) number K903780. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE LAPAROSCOPY ACCESSORY KIT?

AUTO SUTURE LAPAROSCOPY ACCESSORY KIT is a medical device that received FDA 510(k) clearance on 1990-10-23. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K903780.

When did AUTO SUTURE LAPAROSCOPY ACCESSORY KIT receive FDA 510(k) clearance?

AUTO SUTURE LAPAROSCOPY ACCESSORY KIT received FDA 510(k) clearance on 1990-10-23, under 510(k) number K903780.

Who is the listed applicant for AUTO SUTURE LAPAROSCOPY ACCESSORY KIT?

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 LAPAROSCOPY ACCESSORY KIT?

The FDA product code for AUTO SUTURE LAPAROSCOPY ACCESSORY KIT is HET.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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