Cleared Traditional

K760524 - CATHETER CONNECTOR, ARGYLE TUBING
(FDA 510(k) Clearance)

K760524 · Sherwood Medical Industries · General & Plastic Surgery device

Nov 1976

Decision

68d

Days

Class 1

Risk

K760524 is an FDA 510(k) clearance for the CATHETER CONNECTOR, ARGYLE TUBING. This device is classified as a Connector, Catheter (Class I - General Controls, product code GCD).

Submitted by Sherwood Medical Industries (Mchenry, US). The FDA issued a Cleared decision on November 2, 1976, 68 days after receiving the submission on August 26, 1976.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4200.

Submission Details

510(k) Number	K760524 FDA.gov
FDA Decision	Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received	August 26, 1976
Decision Date	November 02, 1976
Days to Decision	68 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—