POWERMATIC TREATMENT TABLE— 510(k) K933581

Name: FDA 510(k) clearance K933581
Creator: U.S. Food and Drug Administration
Published: 1993-11-05

Substantially Equivalent

Medical Device Inspection Co., Inc.

FDA 510(k) clearance K933581 for POWERMATIC TREATMENT TABLE, Substantially Equivalent on 1993-11-05. Applicant: Medical Device Inspection Co., Inc.. Device class: 1.

Clearance details

Applicant: Medical Device Inspection Co., Inc.
Product code: Code INQ
Device class: Class 1
Regulation: 21 CFR 890.3760
Advisory panel: Physical Medicine
Date received: 1993-07-22
Decision date: 1993-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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K933578 — POWERMATIC MAT PLATFORM1993-11-05
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