FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM, MODEL WHF-314 (POWER-Q1000)

K Number: K080134 · Decision Jan 23, 2009
Classifications
1
FEI Numbers
95
Registration Numbers
95
Same Product Code
152
Applicant Total
5
Review Days
371

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Basic Information

Device Name
COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM, MODEL WHF-314 (POWER-Q1000)
K Number
K080134
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5650
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wonjin Mulsan Co., Ltd.
Date Received
January 18, 2008
Decision Date
January 23, 2009
Product Code
IRP
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IRP Massager, Powered Inflatable Tube

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K Number Device Name
K211283 Compressible Limb and Circulation Therapy System, Model POWER-Q2300
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K113275 COMPRESSIBLE LIMB THERAPY SYSTEM
K100656 COMPRESSIBLE LIMB THERAPY SYSTEM MODEL WHF-324 (POWER-Q1000 PLUS)