Rapid Single/Multi-drug Test Cup, Rapid Single/Multi-drug Test Dipcard— 510(k) K153050
Substantially EquivalentCo-Innovation Biotech Co., Ltd.
FDA 510(k) clearance K153050 for Rapid Single/Multi-drug Test Cup, Rapid Single/Multi-drug Test Dipcard, Substantially Equivalent on 2016-04-26. Applicant: Co-Innovation Biotech Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Co-Innovation Biotech Co., Ltd.
- Product code
- Code DJG
- Device class
- Class 2
- Regulation
- 21 CFR 862.3650
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Guangzhou, CN
Recent devices under product code DJG
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Data sourced from openFDA. This site is unofficial and independent of the FDA.