GENESIS MEDICAL TECHNOLOGIES, INC. PHARMAJET NEEDLE-FREE INJECTOR, MODEL M2000— 510(k) K041239
Substantially EquivalentGenesis Medical Technology, Inc.
FDA 510(k) clearance K041239 for GENESIS MEDICAL TECHNOLOGIES, INC. PHARMAJET NEEDLE-FREE INJECTOR, MODEL M2000, Substantially Equivalent on 2004-11-08. Applicant: Genesis Medical Technology, Inc.. Device class: 2.
Clearance details
- Applicant
- Genesis Medical Technology, 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
- Las Vegas, NV, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.