ABBOTT RF EIA DIAGNOSTIC KIT— 510(k) K850373
Substantially EquivalentAbbott Laboratories
FDA 510(k) clearance K850373 for ABBOTT RF EIA DIAGNOSTIC KIT, Substantially Equivalent on 1985-03-01. Applicant: Abbott Laboratories.
Clearance details
- Applicant
- Abbott Laboratories
- Product code
- Code DHR
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Abbott Park, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.