FDA 510(k) Applications for Medical Device Product Code "BYT"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K072290 | DIMA ITALIA SRL | PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUS | 05/29/2008 |
K082657 | MEDIVENT LIMITED | RTX RESPIRATOR | 10/08/2008 |