INTERMITTENT PNEUMATIC COMPRESSION DEVICE— 510(k) K123830

Name: FDA 510(k) clearance K123830
Creator: U.S. Food and Drug Administration
Published: 2013-08-16

Substantially Equivalent

Dalian Labtek Science & Development Co., Ltd.

FDA 510(k) clearance K123830 for INTERMITTENT PNEUMATIC COMPRESSION DEVICE, Substantially Equivalent on 2013-08-16. Applicant: Dalian Labtek Science & Development Co., Ltd.. Device class: 2.

Clearance details

Applicant: Dalian Labtek Science & Development Co., Ltd.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2012-12-12
Decision date: 2013-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shanghai, CN

Download summary PDF View on FDA.gov ↗

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