FDA 510(k) Applications Submitted by AMERIFLO CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K060382 | 02/14/2006 | FLO-RITE, MODEL 478-1; FLO-RITE II, MODEL 478-1; SIMPULSE II, MODEL 478-2S; NUMATIX, MODEL NCD401; SIMPULSE, MODEL 478-1 | AMERIFLO CORP. |
| K041057 | 04/23/2004 | FLO-RITE | AMERIFLO CORP. |
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