The following data is part of a premarket notification filed by Gen-probe Prodesse, Inc with the FDA for Prodesse Proadeno.
| Device ID | K102952 |
| 510k Number | K102952 |
| Device Name: | PRODESSE PROADENO |
| Classification | Respiratory Virus Panel Nucleic Acid Assay System |
| Applicant | GEN-PROBE PRODESSE, INC W229 N1870 WESTWOOD DR Waukesha, WI 53186 |
| Contact | Emily Zielger |
| Correspondent | Emily Zielger GEN-PROBE PRODESSE, INC W229 N1870 WESTWOOD DR Waukesha, WI 53186 |
| Product Code | OCC |
| CFR Regulation Number | 866.3980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-10-05 |
| Decision Date | 2010-12-03 |
| Summary: | summary |