Endocardial Solutions, Inc.
Endocardial Solutions, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2004.
Top product codes for Endocardial Solutions, Inc.
Recent clearances by Endocardial Solutions, Inc.
- K042493 — ENSITE SYSTEM, MODEL EE3000
- K033211 — ENSITE SYSTEM
- K030129 — MODIFICATION TO ENSITE 3000 SYSTEM, MODEL EE3000
- K012926 — MODIFICATION TO ENSITE 3000 SYSTEM, MODEL EE3000
- K001437 — ENSITE 3000 SYSTEM, MODEL EE3000
- K993376 — ENSTYLET MODELS EC0010, EC0020
- K992479 — ENSITE 3000 SYSTEM
- K983456 — ENSITE 3000 SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.