MODIFICATION TO PROFLU+ ASSAY
FDA 510(k) clearance K092500 · decided 2009-08-20
Clearance details
- K-number
- K092500
- Device name
- MODIFICATION TO PROFLU+ ASSAY
- Applicant
- Prodesse, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2009-08-14
- Decision date
- 2009-08-20
- Days to decision
- 6 days
- Clearance type
- Special
- Product code
- OCC
- 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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Recalls involving this device
No recalls on record reference this clearance.