FDA 510(k) Applications Submitted by ARQUILLA, INC. DBA X-CEL X-RAY CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160857 | 03/29/2016 | HF 718BD X-Ray System | ARQUILLA, INC. DBA X-CEL X-RAY CORPORATION |
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