FDA 510(k) Application Details - K882724

Device Classification Name	Drape, Surgical   More FDA Info for this Device
510(K) Number	K882724
Device Name	MICROTEK PROBE DRAPE
Applicant	MICROBIO-MEDICS, INC. POST OFFICE BOX 2487 COLUMBUS, MS 39704 Other 510(k) Applications for this Company   More Company Info and Competitors
Contact	KEITH MCGEE Other 510(k) Applications for this Contact
Regulation Number	878.4370   More FDA Info for this Regulation Number
Classification Product Code	KKX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/01/1988
Decision Date	08/03/1988
Decision	SE - Substantially Equivalent
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type	Traditional
Reviewed By Third Party	N
Expedited Review