SIMULSCOPE AUSCULTATION AND SIMULSCOPE BEDSIDE AUSCULTATION SYSTEM— 510(k) K961937
Substantially EquivalentDelphi Consulting Group
FDA 510(k) clearance K961937 for SIMULSCOPE AUSCULTATION AND SIMULSCOPE BEDSIDE AUSCULTATION SYSTEM, Substantially Equivalent on 1996-12-09. Applicant: Delphi Consulting Group.
Clearance details
- Applicant
- Delphi Consulting Group
- Product code
- Code DQD
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.