Cleared Traditional

POWERMATIC MAT PLATFORM

K933578 · Medical Device Inspection Co., Inc. · Physical Medicine
Nov 1993
Decision
106d
Days
Class 1
Risk

About This 510(k) Submission

K933578 is an FDA 510(k) clearance for the POWERMATIC MAT PLATFORM, 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 November 5, 1993, 106 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 K933578 FDA.gov
FDA Decision Cleared SESE
Date Received July 22, 1993
Decision Date November 05, 1993
Days to Decision 106 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

Similar Devices — INQ Table, Powered

All 101
CARDON PHYSICAL THERAPY TABLE MODEL R28598
K960332 · Cardon Rehabilitation Products, Inc. · Feb 1996
CARDON PHYSICAL THERAPY TABLE MODEL R27116
K960334 · Cardon Rehabilitation Products, Inc. · Feb 1996
CARDON PHYSICAL THERAPY TABLE MODEL R27645
K960336 · Cardon Rehabilitation Products, Inc. · Feb 1996
TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777
K960196 · Tri W-G, Inc. · Feb 1996
EVT-3300
K953621 · U.S. Table, Inc. · Nov 1995
PTT 6200 ELEVATION THERAPY TABLE
K953622 · U.S. Table, Inc. · Sep 1995