FDA 510(k) Applications Submitted by SOL SOROCA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K072479 | 09/04/2007 | FLEXITE SUPREME, FLEXITE PLUS, FLEXITE M.P., NORTHERN AND FLEXITE PRO-GUARD | RAPID INJECTION SYSTEMS CORP. |
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