510(k) K951130
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