BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM— 510(k) K121270
Substantially EquivalentBioject Medical Technologies, Inc.
FDA 510(k) clearance K121270 for BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM, Substantially Equivalent on 2012-07-19. Applicant: Bioject Medical Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Bioject Medical Technologies, Inc.
- 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
- Tigard, OR, US
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More clearances from Bioject Medical Technologies, Inc.
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