FDA 510(k) Applications Submitted by DIACOR, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K050888 | 04/07/2005 | INTEGRA IMMOBILIZATION SYSTEM | DIACOR, INC. |
| K121929 | 07/02/2012 | ZEPHYR 'X-SERIES PATIENT TRANSFER SLED | DIACOR, INC. |
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