ARCHITECT IVANCOMYCIN REAGENTS AND ARCHITECT IVANCOMYCIN CALIBRATORS, MODELS: 1P30-25 AND 1P30-01
FDA 510(k) clearance K072036 · decided 2008-03-19
Clearance details
- K-number
- K072036
- Device name
- ARCHITECT IVANCOMYCIN REAGENTS AND ARCHITECT IVANCOMYCIN CALIBRATORS, MODELS: 1P30-25 AND 1P30-01
- Applicant
- Biokit, S.A.
- Decision
- Substantially Equivalent
- Date received
- 2007-07-25
- Decision date
- 2008-03-19
- Days to decision
- 238 days
- Clearance type
- Traditional
- Product code
- LEH
- Device class
- 2
- Regulation number
- 862.3950
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- Location
- Barcelona, ES
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| ARCHITECT iVancomycin Reagent; an in vitro chemiluminescent microparticle immunoassay (CMI recall (Z-0629-2011) | Abbott Laboratories | 2010-12-16 |