CR3 Keyless Split Sample Cup Secobarbital- Methadone
FDA 510(k) clearance K143535 · decided 2015-01-13
Clearance details
- K-number
- K143535
- Device name
- CR3 Keyless Split Sample Cup Secobarbital- Methadone
- Applicant
- Guangzhou Wondfo Biotech Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2014-12-15
- Decision date
- 2015-01-13
- Days to decision
- 29 days
- Clearance type
- Traditional
- Product code
- DIS
- Device class
- 2
- Regulation number
- 862.3150
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- Location
- Guangzhou, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.