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FDA 510(k) Application Details - K962855
Device Classification Name
Exerciser, Measuring
More FDA Info for this Device
510(K) Number
K962855
Device Name
Exerciser, Measuring
Applicant
PENNY AND GILES BIOMETRICS LTD.
NEWBRIDGE ROAD, BLACKWOOD
GWENT, WALES NP2 2YD GB
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Contact
IAN THOMAS
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Regulation Number
890.5360
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Classification Product Code
ISD
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More FDA Info for this Product Code
Date Received
07/22/1996
Decision Date
12/11/1996
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
N
Expedited Review
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