VASCULIZER— 510(k) K791418
Substantially EquivalentDiagnostics Intl.
FDA 510(k) clearance K791418 for VASCULIZER, Substantially Equivalent on 1979-10-04. Applicant: Diagnostics Intl.. Device class: 2.
Clearance details
- Applicant
- Diagnostics Intl.
- 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
- Mchenry, IL, US
Recent devices under product code DPW
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