CAPPEL DIAGNOSTICS ANA KIT— 510(k) K862821
Substantially EquivalentCappel Diagnostics, Inc.
FDA 510(k) clearance K862821 for CAPPEL DIAGNOSTICS ANA KIT, Substantially Equivalent on 1986-08-15. Applicant: Cappel Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- Cappel Diagnostics, Inc.
- Product code
- Code DHN
- Device class
- Class 2
- Regulation
- 21 CFR 866.5100
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Davis, CA, US
Recent devices under product code DHN
view allMore clearances from Cappel Diagnostics, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.