FDA 510(k) Applications Submitted by DIGITEC MEDICAL SERVICE CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K993681 | 11/01/1999 | DIGITEC TWO STAGE COMPRESSION KIT | DIGITEC MEDICAL SERVICE CORP. |
| K010792 | 03/16/2001 | MAMMOGRAPH | DIGITEC MEDICAL SERVICE CORP. |
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