FDA 510(k) Applications Submitted by KEITH CRAWFORD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K992132 | 06/23/1999 | CHOLESITE TEST SYSTEM | GDS TECHNOLOGY, LLC. |
| K994073 | 12/02/1999 | HEMOSITE TEST SYSTEM | GDS TECHNOLOGY, LLC. |
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