FDA 510(k) Applications Submitted by CURTIS VAN ALLEN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K973454 | 09/11/1997 | AD-TECH'S SPINAL ELECTRODE | AD-TECH MEDICAL INSTRUMENT CORP. |
| K970587 | 02/18/1997 | AD-TECH SUBDURAL ELECTRODE | AD-TECH MEDICAL INSTRUMENT CORP. |
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