THE FREEDOM BED— 510(k) K954671

Name: FDA 510(k) clearance K954671
Creator: U.S. Food and Drug Administration
Published: 1996-04-01

Substantially Equivalent

Probed Medical Technologies, Inc.

FDA 510(k) clearance K954671 for THE FREEDOM BED, Substantially Equivalent on 1996-04-01. Applicant: Probed Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Probed Medical Technologies, Inc.
Product code: Code IKZ
Device class: Class 2
Regulation: 21 CFR 890.5225
Advisory panel: Physical Medicine
Date received: 1995-10-10
Decision date: 1996-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chilliwack, B.C., CA

Download summary PDF View on FDA.gov ↗

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