MODIFICATION OF EMIT D.A.U. OPIATES ASSAY
FDA 510(k) clearance K984232 · decided 1999-01-22
Clearance details
- K-number
- K984232
- Device name
- MODIFICATION OF EMIT D.A.U. OPIATES ASSAY
- Applicant
- Syva Co.
- Decision
- Substantially Equivalent
- Date received
- 1998-11-25
- Decision date
- 1999-01-22
- Days to decision
- 58 days
- Clearance type
- Traditional
- Product code
- DJG
- Device class
- 2
- Regulation number
- 862.3650
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- Location
- San Jose, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.