MODEL 2100 FETAL MONITOR— 510(k) K837102
Substantially EquivalentHuntleigh Group , Ltd.
FDA 510(k) clearance K837102 for MODEL 2100 FETAL MONITOR, Substantially Equivalent on 1983-03-14. Applicant: Huntleigh Group , Ltd..
Clearance details
- Applicant
- Huntleigh Group , Ltd.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Luton Beds Lu1 1uu, GB
Data sourced from openFDA. This site is unofficial and independent of the FDA.