FDA 510(k) Applications Submitted by CANDULOR USA, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K101814 | 06/29/2010 | DIRECT CROWN NATURAL 1 | CANDULOR USA, INC. |
| K122852 | 09/18/2012 | PHYSIOSTAR NFC | CANDULOR USA, INC. |
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