FUTREX-6100/XL— 510(k) K963271
Substantially EquivalentFutrex, Inc.
FDA 510(k) clearance K963271 for FUTREX-6100/XL, Substantially Equivalent on 1998-08-19. Applicant: Futrex, Inc.. Device class: 2.
Clearance details
- Applicant
- Futrex, Inc.
- Product code
- Code MNW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2770
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Gaithersburg, MD, US
Recent devices under product code MNW
view allMore clearances from Futrex, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.