FHB, FHB-T, FHBFLEX, FHBFLEX-T— 510(k) K925622
Substantially EquivalentIcor AB
FDA 510(k) clearance K925622 for FHB, FHB-T, FHBFLEX, FHBFLEX-T, Substantially Equivalent on 1993-05-26. Applicant: Icor AB.
Clearance details
- Applicant
- Icor AB
- Product code
- Code BYD
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bromma, SE
Data sourced from openFDA. This site is unofficial and independent of the FDA.