FDA 510(k) Applications Submitted by SCHILLER AMERICA, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970879 | 03/10/1997 | CARDIOVIT CS-200 | SCHILLER AMERICA, INC. |
| K973735 | 09/30/1997 | MICROVIT MT-100 | SCHILLER AMERICA, INC. |
| K973751 | 10/01/1997 | MT-200 | SCHILLER AMERICA, INC. |
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