Medline ReNewal Reprocessed Compression Limb Sleeves— 510(k) K143166

Name: FDA 510(k) clearance K143166
Creator: U.S. Food and Drug Administration
Published: 2015-01-16

Substantially Equivalent

Surgical Instrument Service and Savings (Dba Medline Renewal

FDA 510(k) clearance K143166 for Medline ReNewal Reprocessed Compression Limb Sleeves, Substantially Equivalent on 2015-01-16. Applicant: Surgical Instrument Service and Savings (Dba Medline Renewal. Device class: 2.

Clearance details

Applicant: Surgical Instrument Service and Savings (Dba Medline Renewal
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2014-11-04
Decision date: 2015-01-16
Decision: Substantially Equivalent
Clearance type: Special
Location: Redmond, OR, US

Download summary PDF View on FDA.gov ↗

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