DUFFY BOLUS INJECTOR— 510(k) K863936
Substantially EquivalentViox Corp.
FDA 510(k) clearance K863936 for DUFFY BOLUS INJECTOR, Substantially Equivalent on 1987-01-06. Applicant: Viox Corp.. Device class: 1.
Clearance details
- Applicant
- Viox Corp.
- Product code
- Code IWR
- Device class
- Class 1
- Regulation
- 21 CFR 892.6500
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Seattle, WA, US
Recent devices under product code IWR
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