FDA 510(k) Applications Submitted by MICHIGAN INSTRUMENTS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K073079 | 10/31/2007 | THUMPER, MODEL: 1008 | MICHIGAN INSTRUMENTS, INC. |
| K962237 | 06/11/1996 | THUMPER CARDIOPULMONARY RESUSCITATOR | MICHIGAN INSTRUMENTS, INC. |
| K972525 | 07/07/1997 | THUMPER | MICHIGAN INSTRUMENTS, INC. |
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