ARTICULAR MOTION DEVICE (AMD4000)— 510(k) K863639

Name: FDA 510(k) clearance K863639
Creator: U.S. Food and Drug Administration
Published: 1986-09-29

Substantially Equivalent

Med Surg Designs, Inc.

FDA 510(k) clearance K863639 for ARTICULAR MOTION DEVICE (AMD4000), Substantially Equivalent on 1986-09-29. Applicant: Med Surg Designs, Inc.. Device class: 1.

Clearance details

Applicant: Med Surg Designs, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1986-09-17
Decision date: 1986-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chardon, OH, US

Download summary PDF View on FDA.gov ↗

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