IF-II (TM), MODEL 9800— 510(k) K883462
Substantially EquivalentMedical Devices, Inc.
FDA 510(k) clearance K883462 for IF-II (TM), MODEL 9800, Substantially Equivalent on 1989-05-24. Applicant: Medical Devices, Inc..
Clearance details
- Applicant
- Medical Devices, Inc.
- Product code
- Code LIH
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Paul, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.