510(k) K951130

CARDIOSOFT/CARDIOSYS by Marquette Electronics, Inc. — Product Code LOS

K951130 is an FDA 510(k) premarket notification submitted by Marquette Electronics, Inc. for the device "CARDIOSOFT/CARDIOSYS". The FDA issued a decision of Substantially Equivalent on April 4, 1996. Marquette Electronics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 4, 1996
Date Received
March 13, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No