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FDA 510(k) Application Details - K102783
Device Classification Name
Wrap, Sterilization
More FDA Info for this Device
510(K) Number
K102783
Device Name
Wrap, Sterilization
Applicant
HINSON AND HALE MEDICAL TECHNOLOGIES, INC
7809 ADELAIDE DRIVE
AUSTIN, TX 78739 US
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Contact
JEFFREY O STULL
Other 510(k) Applications for this Contact
Regulation Number
880.6850
More FDA Info for this Regulation Number
Classification Product Code
FRG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/27/2010
Decision Date
12/22/2010
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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