FDA 510(k) Application Details - K990412

Device Classification Name	Blood Pressure Cuff   More FDA Info for this Device
510(K) Number	K990412
Device Name	Blood Pressure Cuff
Applicant	VITAL SIGNS, INC. 20 CAMPUS RD. TOTOWA, NJ 07512 US Other 510(k) Applications for this Company
Contact	ANTHONY P MARTINO Other 510(k) Applications for this Contact
Regulation Number	870.1120   More FDA Info for this Regulation Number
Classification Product Code	DXQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/10/1999
Decision Date	09/01/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review