VITAJET— 510(k) K962625
Substantially EquivalentVitajet Corp.
FDA 510(k) clearance K962625 for VITAJET, Substantially Equivalent on 1996-12-10. Applicant: Vitajet Corp.. Device class: 2.
Clearance details
- Applicant
- Vitajet Corp.
- Product code
- Code KZE
- Device class
- Class 2
- Regulation
- 21 CFR 880.5430
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Laguna Hills, CA, US
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More clearances from Vitajet Corp.
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