SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES— 510(k) K052691

Name: FDA 510(k) clearance K052691
Creator: U.S. Food and Drug Administration
Published: 2006-05-17

Substantially Equivalent

Suretek Medical

FDA 510(k) clearance K052691 for SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES, Substantially Equivalent on 2006-05-17. Applicant: Suretek Medical. Device class: 2.

Clearance details

Applicant: Suretek Medical
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2005-09-28
Decision date: 2006-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Greenville, SC, US

Download summary PDF View on FDA.gov ↗

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