MONITORING SYSTEM, MODEL ARGUS PB-2200— 510(k) K033738
Substantially EquivalentSchiller AG
FDA 510(k) clearance K033738 for MONITORING SYSTEM, MODEL ARGUS PB-2200, Substantially Equivalent on 2004-08-24. Applicant: Schiller AG.
Clearance details
- Applicant
- Schiller AG
- Product code
- Code DSK
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Baar, CH
Data sourced from openFDA. This site is unofficial and independent of the FDA.