FDA 510(k) Applications Submitted by PATRICIA M HOJNOSKI
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K113181 | 10/28/2011 | CELLTRACKS ANALYER II | VERIDEX, LLC |
| K040302 | 02/09/2004 | VERSAPOINT RESECTOSCOPIC SYSTEM | GYNECARE, A DIV. OF ETHICON, INC. |
| K052401 | 09/01/2005 | GYNECARE TVT SECUR SYSTEM | ETHICON, INC. |
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