IMMUNOCAP ALLERGEN K82
FDA 510(k) clearance K121463 · decided 2013-01-29
Clearance details
- K-number
- K121463
- Device name
- IMMUNOCAP ALLERGEN K82
- Applicant
- Thermo Fisher Scientific
- Decision
- Substantially Equivalent
- Date received
- 2012-05-17
- Decision date
- 2013-01-29
- Days to decision
- 257 days
- Clearance type
- Traditional
- Product code
- DHB
- Device class
- 2
- Regulation number
- 866.5750
- Medical specialty
- Immunology
- Advisory committee
- Immunology
- Location
- Portage, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instru recall (Z-0947-2015) | Phadia US Inc | 2015-01-12 |