E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120— 510(k) K961301
Substantially EquivalentDelphi Consulting Group
FDA 510(k) clearance K961301 for E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120, Substantially Equivalent on 1996-06-11. Applicant: Delphi Consulting Group. Device class: 2.
Clearance details
- Applicant
- Delphi Consulting Group
- Product code
- Code DQD
- Device class
- Class 2
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
Recent devices under product code DQD
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