A1-A2 AMBULATORY EEG CASSETTE RECORDER— 510(k) K870432
Substantially EquivalentGrass-Telefactor Product Group
FDA 510(k) clearance K870432 for A1-A2 AMBULATORY EEG CASSETTE RECORDER, Substantially Equivalent on 1987-05-08. Applicant: Grass-Telefactor Product Group.
Clearance details
- Applicant
- Grass-Telefactor Product Group
- Product code
- Code GWQ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- W. Conshohocken, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.