FDA 510(k) Applications Submitted by PIERRE LEMIRE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K071086 | 04/17/2007 | RESOLUTIONMD CARDIAC PRODUCT FAMILY, MODEL: RELEASE 1.0 | CALGARY SCIENTIFIC, INC. |
| K062164 | 07/28/2006 | RESOLUTIONMD, VERSION 1.3 | CALGARY SCIENTIFIC, INC. |
| K082693 | 09/15/2008 | RESOLUTIONMD, RELEASE 2.1 | CALGARY SCIENTIFIC, INC. |
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