510(k) K991735
K991735 is an FDA 510(k) premarket notification submitted by General Electric Medical Systems Information Techn for the device "MAC SERIES ELECTROCARDIOGRAPHS INCLUDING MAC 5000, MAC PC, MAC 6, MAC VU, MAC 8 ELECTROCARDIOGRAPHS". The FDA issued a decision of Substantially Equivalent on August 19, 1999. General Electric Medical Systems Information Techn has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 19, 1999
- Date Received
- May 21, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No