INTERMITTENT PNEUMATIC COMPRESSION DEVICE— 510(k) K141390

Name: FDA 510(k) clearance K141390
Creator: U.S. Food and Drug Administration
Published: 2014-11-18

Substantially Equivalent

Wuhan Landing Medical Hi-Tech, Ltd.

FDA 510(k) clearance K141390 for INTERMITTENT PNEUMATIC COMPRESSION DEVICE, Substantially Equivalent on 2014-11-18. Applicant: Wuhan Landing Medical Hi-Tech, Ltd.. Device class: 2.

Clearance details

Applicant: Wuhan Landing Medical Hi-Tech, Ltd.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2014-05-27
Decision date: 2014-11-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wuham, CN

Download summary PDF View on FDA.gov ↗

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