RUBELISA IGM TEST KIT— 510(k) K802508
Substantially EquivalentM.A. Bioproducts
FDA 510(k) clearance K802508 for RUBELISA IGM TEST KIT, Substantially Equivalent on 1980-12-18. Applicant: M.A. Bioproducts.
Clearance details
- Applicant
- M.A. Bioproducts
- Product code
- Code GOL
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.