RF1400 Active Compression Wrap— 510(k) K162481

Name: FDA 510(k) clearance K162481
Creator: U.S. Food and Drug Administration
Published: 2017-02-16

Substantially Equivalent

Recovery Force, LLC

FDA 510(k) clearance K162481 for RF1400 Active Compression Wrap, Substantially Equivalent on 2017-02-16. Applicant: Recovery Force, LLC. Device class: 2.

Clearance details

Applicant: Recovery Force, LLC
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2016-09-06
Decision date: 2017-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fishers, IN, US

Download summary PDF View on FDA.gov ↗

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