FDA 510(k) Applications Submitted by HEYER AMERICA, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000995 | 03/28/2000 | NARKOMAT, MODEL 2000 | HEYER AMERICA, INC. |
| K001988 | 06/29/2000 | MODULAR | HEYER AMERICA, INC. |
| K963481 | 09/03/1996 | ANODYNE CC | HEYER AMERICA, INC. |
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