AUTO SUTURE(R) ENDOSCOPIC CLAMP— 510(k) K903205

Name: FDA 510(k) clearance K903205
Creator: U.S. Food and Drug Administration
Published: 1990-10-11

Substantially Equivalent

United States Surgical, A Division of Tyco Healthc

FDA 510(k) clearance K903205 for AUTO SUTURE(R) ENDOSCOPIC CLAMP, Substantially Equivalent on 1990-10-11. Applicant: United States Surgical, A Division of Tyco Healthc. Device class: 2.

Clearance details

Applicant: United States Surgical, A Division of Tyco Healthc
Product code: Code HDA
Device class: Class 2
Regulation: 21 CFR 884.4400
Advisory panel: Obstetrics/Gynecology
Date received: 1990-07-20
Decision date: 1990-10-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

Download summary PDF View on FDA.gov ↗

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Recalls naming K903205

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K903205.

Data sourced from openFDA. This site is unofficial and independent of the FDA.