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FDA 510(k) Application Details - K973340
Device Classification Name
Epilator, High Frequency, Tweezer-Type
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510(K) Number
K973340
Device Name
Epilator, High Frequency, Tweezer-Type
Applicant
MOBIT, INC.
420 LEXINGTON AVE.
NEW YORK, NY 10170 US
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Contact
JAMES R MARSHALL
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Regulation Number
878.5360
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Classification Product Code
KCX
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More FDA Info for this Product Code
Date Received
09/05/1997
Decision Date
12/03/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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