Cleared Traditional

THE HILL ADJUSTABLE PODIATRY MODEL

K952357 · Hill Laboratories Co. · Physical Medicine
Jul 1995
Decision
70d
Days
Class 1
Risk

About This 510(k) Submission

K952357 is an FDA 510(k) clearance for the THE HILL ADJUSTABLE PODIATRY MODEL, a Table, Powered (Class I — General Controls, product code INQ), submitted by Hill Laboratories Co. (Malvern, US). The FDA issued a Cleared decision on July 6, 1995, 70 days after receiving the submission on April 27, 1995. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K952357 FDA.gov
FDA Decision Cleared SESE
Date Received April 27, 1995
Decision Date July 06, 1995
Days to Decision 70 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF

Device Classification

Product Code INQ — Table, Powered
Device Class Class I — General Controls
CFR Regulation 21 CFR 890.3760

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