FDA 510(k) Applications Submitted by LUMISCOPE CO., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K032714 | 09/02/2003 | CARDICARE MODEL MT-301F & MT-301C | LUMISCOPE CO., INC. |
| K954792 | 10/18/1995 | LUMISCOPE MODEL 2018 THERMOMETER | LUMISCOPE CO., INC. |
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