Rapid Single/Multi-drug Test Cup and Rapid Single/Multi-drug Test Dipcard— 510(k) K142800
Substantially EquivalentCo-Innovation Biotech Co., Ltd.
FDA 510(k) clearance K142800 for Rapid Single/Multi-drug Test Cup and Rapid Single/Multi-drug Test Dipcard, Substantially Equivalent on 2014-12-11. Applicant: Co-Innovation Biotech Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Co-Innovation Biotech Co., Ltd.
- Product code
- Code DKZ
- Device class
- Class 2
- Regulation
- 21 CFR 862.3100
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Guangzhou, CN
Recent devices under product code DKZ
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Data sourced from openFDA. This site is unofficial and independent of the FDA.