Rapid Single/Multi-drug Test Cup, Rapid Single/Multi-drug Test Dipcard
FDA 510(k) clearance K153050 · decided 2016-04-26
Clearance details
- K-number
- K153050
- Device name
- Rapid Single/Multi-drug Test Cup, Rapid Single/Multi-drug Test Dipcard
- Applicant
- Co-Innovation Biotech Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2015-10-20
- Decision date
- 2016-04-26
- Days to decision
- 189 days
- Clearance type
- Special
- Product code
- DJG
- Device class
- 2
- Regulation number
- 862.3650
- 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.