QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121
FDA 510(k) clearance K043051 · decided 2005-02-07
Clearance details
- K-number
- K043051
- Device name
- QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121
- Applicant
- Phamatech, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2004-11-04
- Decision date
- 2005-02-07
- Days to decision
- 95 days
- Clearance type
- Traditional
- Product code
- DJG
- Device class
- 2
- Regulation number
- 862.3650
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- Location
- San Diego, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.