Cleared Traditional

POWERMATIC EXAMINATION TABLE

K933577 · Medical Device Inspection Co., Inc. · Physical Medicine
Sep 1993
Decision
70d
Days
Class 1
Risk

About This 510(k) Submission

K933577 is an FDA 510(k) clearance for the POWERMATIC EXAMINATION TABLE, a Table, Powered (Class I — General Controls, product code INQ), submitted by Medical Device Inspection Co., Inc. (Great Neck, US). The FDA issued a Cleared decision on September 30, 1993, 70 days after receiving the submission on July 22, 1993. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3760.

Submission Details

510(k) Number K933577 FDA.gov
FDA Decision Cleared SESE
Date Received July 22, 1993
Decision Date September 30, 1993
Days to Decision 70 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement

Device Classification

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

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