DIAGNOSTIC ULTRASOUND VERSADOPP 1000— 510(k) K904792
Substantially EquivalentDiagnostic Ultrasound Corp.
FDA 510(k) clearance K904792 for DIAGNOSTIC ULTRASOUND VERSADOPP 1000, Substantially Equivalent on 1991-01-28. Applicant: Diagnostic Ultrasound Corp.. Device class: 2.
Clearance details
- Applicant
- Diagnostic Ultrasound Corp.
- Product code
- Code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kirkland, WA, US
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