FDA 510(k) Application Details - K951722

Device Classification Name	Transducer, Blood-Pressure, Extravascular   More FDA Info for this Device
510(K) Number	K951722
Device Name	Transducer, Blood-Pressure, Extravascular
Applicant	NAMIC PRUYNS ISLAND GLENS FALLS, NY 12801 US Other 510(k) Applications for this Company
Contact	MARY M RUBIN Other 510(k) Applications for this Contact
Regulation Number	870.2850   More FDA Info for this Regulation Number
Classification Product Code	DRS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/14/1995
Decision Date	03/25/1996
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