MULTI DOPPLEX, MD-1— 510(k) K900882
Substantially EquivalentHuntleigh Technology, Inc.
FDA 510(k) clearance K900882 for MULTI DOPPLEX, MD-1, Substantially Equivalent on 1990-08-22. Applicant: Huntleigh Technology, Inc.. Device class: 2.
Clearance details
- Applicant
- Huntleigh Technology, Inc.
- Product code
- Code JAF
- Device class
- Class 2
- Regulation
- 21 CFR 892.1540
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Manalapan, NJ, US
Recent devices under product code JAF
view allMore clearances from Huntleigh Technology, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.