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.. Device class: 2.
Clearance details
- Applicant
- Huntleigh Technology, Inc.
- Product code
- Code KNG
- Device class
- Class 2
- Regulation
- 21 CFR 884.2660
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Manalapan, NJ, US
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