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FDA 510(k) Application Details - K070672
Device Classification Name
Table, Physical Therapy, Multi Function
More FDA Info for this Device
510(K) Number
K070672
Device Name
Table, Physical Therapy, Multi Function
Applicant
METEK GMBH
STAMMWEG 8
LEINEFELDE 37327 DE
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Contact
STEFAN ZIEGENFUB
Other 510(k) Applications for this Contact
Regulation Number
890.5880
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Classification Product Code
JFB
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More FDA Info for this Product Code
Date Received
03/12/2007
Decision Date
06/26/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
Y
Expedited Review
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