FDA 510(k) Applications Submitted by SNOWDEN-PENCER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960400 | 01/29/1996 | DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS) | SNOWDEN-PENCER |
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