FDA 510(k) Applications Submitted by AMERICAN CUSTOM MEDICAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K964656 | 11/20/1996 | TEFGEN GUIDED TISSUE MEMBRANE | AMERICAN CUSTOM MEDICAL, INC. |
| K965205 | 12/26/1996 | TEFGEN - LS | AMERICAN CUSTOM MEDICAL, INC. |
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