FDA 510(k) Application Details - K981393

Device Classification Name	Gown, Surgical   More FDA Info for this Device
510(K) Number	K981393
Device Name	Gown, Surgical
Applicant	KIMBERLY-CLARK CORP. 1400 HOLCOMB BRIDGE RD. ROSWELL, GA 30076 US Other 510(k) Applications for this Company
Contact	LARRY R KLUDT Other 510(k) Applications for this Contact
Regulation Number	878.4040   More FDA Info for this Regulation Number
Classification Product Code	FYA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/17/1998
Decision Date	07/10/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review