FDA 510(k) Application Details - K003052

Device Classification Name	Catheter, Angioplasty, Peripheral, Transluminal   More FDA Info for this Device
510(K) Number	K003052
Device Name	Catheter, Angioplasty, Peripheral, Transluminal
Applicant	NUMED, INC. P.O BOX 129 NICHOLVILLE, NY 12965 US Other 510(k) Applications for this Company
Contact	NICHELLE R LAFLESH Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	LIT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/02/2000
Decision Date	11/01/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review