DERATA MEDI-JECTOR III— 510(k) K844111
Substantially EquivalentDerata Corp.
FDA 510(k) clearance K844111 for DERATA MEDI-JECTOR III, Substantially Equivalent on 1984-11-28. Applicant: Derata Corp.. Device class: 2.
Clearance details
- Applicant
- Derata 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
- Minneapolis, MN, US
Recent devices under product code KZE
view all- K121270 — BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM
- K111517 — PHARMAJET STRATIS 0.5 ML NEEDLE-FREE INJECTION SYSTEM MODEL 501-01, STRATIS INJECTOR CATALOG 501-10, STRATIS RESET STATI
- K110456 — PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEM
- K090959 — LECTRAJET NEEDLE-FREE INJECTION SYSTEM, MODEL: M3 RA
- K090003 — ZETAJET
More clearances from Derata Corp.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.