HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140— 510(k) K900618
Substantially EquivalentHuntleigh Technology, Inc.
FDA 510(k) clearance K900618 for HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140, Substantially Equivalent on 1990-04-25. Applicant: Huntleigh Technology, Inc..
Clearance details
- Applicant
- Huntleigh Technology, Inc.
- Product code
- Code KNG
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Manalapan, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.