UCP RAPID DRUG SCREENING TRICYCLIC ANTIDEPRESSANT, PROPOXYPHENE TESTS
FDA 510(k) clearance K061457 · decided 2006-08-21
Clearance details
- K-number
- K061457
- Device name
- UCP RAPID DRUG SCREENING TRICYCLIC ANTIDEPRESSANT, PROPOXYPHENE TESTS
- Applicant
- Ucp Biosciences, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2006-05-25
- Decision date
- 2006-08-21
- Days to decision
- 88 days
- Clearance type
- Traditional
- Product code
- LFG
- Device class
- 2
- Regulation number
- 862.3910
- 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.