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FDA 510(k) Application Details - K032955
Device Classification Name
Stimulator, Muscle, Powered
More FDA Info for this Device
510(K) Number
K032955
Device Name
Stimulator, Muscle, Powered
Applicant
DANMETER A/S
KILDEMOSEVEJ 13
ODENSE C DK-5000 DK
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Contact
HANNE NIELSEN
Other 510(k) Applications for this Contact
Regulation Number
890.5850
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Classification Product Code
IPF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/22/2003
Decision Date
12/15/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Statement
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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