LIFEDOP MODEL 300ABI— 510(k) K093393
Substantially EquivalentSummit Doppler Systems, Inc.
FDA 510(k) clearance K093393 for LIFEDOP MODEL 300ABI, Substantially Equivalent on 2009-12-24. Applicant: Summit Doppler Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Summit Doppler Systems, Inc.
- Product code
- Code JAF
- Device class
- Class 2
- Regulation
- 21 CFR 892.1540
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Golden, CO, US
Recent devices under product code JAF
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