AMES THERAPY DEVICE— 510(k) K123746

Substantially Equivalent

Ames Technology, Inc.

FDA 510(k) clearance K123746 for AMES THERAPY DEVICE, Substantially Equivalent on 2013-05-24. Applicant: Ames Technology, Inc..

Clearance details

Applicant: Ames Technology, Inc.
Product code: Code IKK
Advisory panel: Physical Medicine
Date received: 2012-12-06
Decision date: 2013-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eugene, OR, US

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