FDA 510(k) Applications Submitted by Justin Padia
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K131479 | 05/22/2013 | V8 SP NORMAL CONTROL, ABNORMAL CONTROL | HELENA LABORATORIES |
| K192931 | 10/17/2019 | V8 Nexus Hemoglobin Ultrascreen, V8 AFSA2 Hemo Control | Helena Laboratories, Corp. |
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