REWALK— 510(k) DEN130034

Unknown

Argo Medical Technologies, Inc.

FDA 510(k) clearance DEN130034 for REWALK, Unknown on 2014-06-26. Applicant: Argo Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Argo Medical Technologies, Inc.
Product code: Code PHL
Device class: Class 2
Regulation: 21 CFR 890.3480
Advisory panel: Physical Medicine
Date received: 2013-06-17
Decision date: 2014-06-26
Decision: Unknown
Clearance type: Direct
Location: Marlborough, MA, US

View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.