Gen-Probe Prodesse, Inc.
Gen-Probe Prodesse, Inc. appears in FDA public data with 0 recalls, 10 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 26, 2013.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K132237 | PRODESSE PROFAST+ ASSAY | August 26, 2013 |
| K132238 | PROPARAFLU+ ASSAY | August 26, 2013 |
| K132200 | PRO HMPV+ ASSAY | August 14, 2013 |
| K132159 | PROADENO+ ASSAY | August 14, 2013 |
| K132129 | PRODESSE PROFLU+ ASSAY | August 9, 2013 |
| K123838 | PRO HMPV+ ASSAY | January 16, 2013 |
| K123274 | PROGASTRO SSCS ASSAY | January 16, 2013 |
| K110968 | PROFLU+ ASSAY | June 27, 2011 |
| K102952 | PRODESSE PROADENO | December 3, 2010 |
| K101855 | PROFAST+ ASSAY | July 23, 2010 |