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

VECTRA GENISYS VMS FR

K Number: K062354 · Decision Jan 26, 2007
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
81
Review Days
165

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Basic Information

Device Name
VECTRA GENISYS VMS FR
K Number
K062354
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Encore Medical L.P.
Date Received
August 14, 2006
Decision Date
January 26, 2007
Product Code
IPF
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
IPF Stimulator, Muscle, Powered

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