TDX IMMUNOGLOBULIN G DIAGNOSTIC KIT— 510(k) K872800
Substantially EquivalentAbbott Laboratories
FDA 510(k) clearance K872800 for TDX IMMUNOGLOBULIN G DIAGNOSTIC KIT, Substantially Equivalent on 1987-08-12. Applicant: Abbott Laboratories.
Clearance details
- Applicant
- Abbott Laboratories
- Product code
- Code DEW
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irving, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.