PROPARAFLU+ASSAY
FDA 510(k) clearance K091053 · decided 2009-11-20
Clearance details
- K-number
- K091053
- Device name
- PROPARAFLU+ASSAY
- Applicant
- Prodesse, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2009-04-13
- Decision date
- 2009-11-20
- Days to decision
- 221 days
- Clearance type
- Traditional
- Product code
- OOU
- Device class
- 2
- Regulation number
- 866.3980
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- Waukesha, WI, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Panther Fusion Paraflu Assay (K172282) | Hologic, Inc. | 2017-10-23 |
| ProParaFlu+ Assay (K153223) | Hologic, Inc. | 2015-12-09 |
| LYRA PARAINFLUENZA VIRUS ASSAY (K141927) | Quidel Corporation | 2014-10-09 |
| PROPARAFLU+ ASSAY (K132238) | Gen-Probe Prodesse, Inc. | 2013-08-26 |
Recalls involving this device
No recalls on record reference this clearance.