RANDOX ETHANOL ASSAY
FDA 510(k) clearance K092273 · decided 2010-11-01
Clearance details
- K-number
- K092273
- Device name
- RANDOX ETHANOL ASSAY
- Applicant
- Randox Laboratories, Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2009-07-28
- Decision date
- 2010-11-01
- Days to decision
- 461 days
- Clearance type
- Traditional
- Product code
- DIC
- Device class
- 2
- Regulation number
- 862.3040
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- Location
- Crumlin, GB
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.