DUOMED, SERIES 500, (MODELS ID 500, FL 500)— 510(k) K030140
Substantially EquivalentDuomed, Inc.
FDA 510(k) clearance K030140 for DUOMED, SERIES 500, (MODELS ID 500, FL 500), Substantially Equivalent on 2003-03-18. Applicant: Duomed, Inc..
Clearance details
- Applicant
- Duomed, Inc.
- Product code
- Code GZJ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- West Palm Beach, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.