FIAX TEST KIT FOR LYME DISEASE ANTIBODIES— 510(k) K872247
Substantially EquivalentWhittaker Bioproducts, Inc.
FDA 510(k) clearance K872247 for FIAX TEST KIT FOR LYME DISEASE ANTIBODIES, Substantially Equivalent on 1987-10-15. Applicant: Whittaker Bioproducts, Inc..
Clearance details
- Applicant
- Whittaker Bioproducts, Inc.
- Product code
- Code LSR
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walkersville, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.