FDA 510(k) Application Details - K002248

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K002248
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	CRITIKON COMPANY,LLC 4502 WOODLAND CORPORATE BLVD. TAMPA, FL 33614 US Other 510(k) Applications for this Company
Contact	THOMAS J ENGLISH Other 510(k) Applications for this Contact
Regulation Number	870.1130   More FDA Info for this Regulation Number
Classification Product Code	DXN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/25/2000
Decision Date	09/21/2000
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