FDA 510(k) Application Details - K955552

Device Classification Name	Tourniquet, Pneumatic   More FDA Info for this Device
510(K) Number	K955552
Device Name	Tourniquet, Pneumatic
Applicant	SMITH & NEPHEW RICHARDS, INC. 2925 APPLING RD. BARTLETT, TN 38133 US Other 510(k) Applications for this Company
Contact	RONALD K SMITH Other 510(k) Applications for this Contact
Regulation Number	878.5910   More FDA Info for this Regulation Number
Classification Product Code	KCY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/05/1995
Decision Date	01/05/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review