Cleared Traditional

K920579 - LOW PROFILE PASSPORT PUSH & PULL KITS & PEG TUBE (FDA 510(k) Clearance)

Jul 1994
Decision
879d
Days
Class 2
Risk

K920579 is an FDA 510(k) clearance for the LOW PROFILE PASSPORT PUSH & PULL KITS & PEG TUBE. This device is classified as a Tubes, Gastrointestinal (and Accessories) (Class II - Special Controls, product code KNT).

Submitted by Wilson-Cook Medical, Inc. (Winston-Salem, US). The FDA issued a Cleared decision on July 8, 1994, 879 days after receiving the submission on February 10, 1992.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5980.

Submission Details

510(k) Number K920579 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 10, 1992
Decision Date July 08, 1994
Days to Decision 879 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement

Device Classification

Product Code KNT — Tubes, Gastrointestinal (and Accessories)
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.5980