510(k) K912049

SYSTEM ATHENA - PRODUCT ENHANCEMENTS by S & W Medico Teknik — Product Code DRT

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 5, 1991
Date Received
April 9, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Device Class
Class II
Regulation Number
870.2300
Review Panel
CV
Submission Type