POWERMATIC EXAMINATION TABLE— 510(k) K933727

Name: FDA 510(k) clearance K933727
Creator: U.S. Food and Drug Administration
Published: 1994-02-09

Substantially Equivalent

Hausmann Industries, Inc.

FDA 510(k) clearance K933727 for POWERMATIC EXAMINATION TABLE, Substantially Equivalent on 1994-02-09. Applicant: Hausmann Industries, Inc.. Device class: 1.

Clearance details

Applicant: Hausmann Industries, Inc.
Product code: Code INQ
Device class: Class 1
Regulation: 21 CFR 890.3760
Advisory panel: Physical Medicine
Date received: 1993-08-02
Decision date: 1994-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck,, NY, US

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K960334 — CARDON PHYSICAL THERAPY TABLE MODEL R271161996-02-13
K960336 — CARDON PHYSICAL THERAPY TABLE MODEL R276451996-02-13
K960196 — TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 7771996-02-07
K953621 — EVT-33001995-11-14

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