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FDA 510(k) Application Details - K963467
Device Classification Name
Restraint, Protective
More FDA Info for this Device
510(K) Number
K963467
Device Name
Restraint, Protective
Applicant
DEROYAL INDUSTRIES, INC.
200 DEBUSK LN.
POWELL, TN 37849 US
Other 510(k) Applications for this Company
Contact
CAMILLE MATLOCK
Other 510(k) Applications for this Contact
Regulation Number
880.6760
More FDA Info for this Regulation Number
Classification Product Code
FMQ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/03/1996
Decision Date
01/03/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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