Cleared Traditional

STOCKINETTE

K770173 · Chase Mfg. Co. · Physical Medicine
Feb 1977
Decision
13d
Days
Class 1
Risk

About This 510(k) Submission

K770173 is an FDA 510(k) clearance for the STOCKINETTE, a Stocking, Elastic (Class I — General Controls, product code ILG), submitted by Chase Mfg. Co. (Mchenry, US). The FDA issued a Cleared decision on February 8, 1977, 13 days after receiving the submission on January 26, 1977. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3475.

Submission Details

510(k) Number K770173 FDA.gov
FDA Decision Cleared SESE
Date Received January 26, 1977
Decision Date February 08, 1977
Days to Decision 13 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary —

Device Classification

Product Code ILG — Stocking, Elastic
Device Class Class I — General Controls
CFR Regulation 21 CFR 890.3475