FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BIOJECT JET INJECTION SYSTEM

K Number: K920631 · Decision Jun 28, 1994
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
52
Applicant Total
9
Review Days
867

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Basic Information

Device Name
BIOJECT JET INJECTION SYSTEM
K Number
K920631
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5430
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bioject, Inc.
Date Received
February 12, 1992
Decision Date
June 28, 1994
Product Code
KZE
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KZE Injector, Fluid, Non-Electrically Powered

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K003908 SEROJET
K994384 CLICKER
K960373 BIOJECTOR 2000 MODEL 1B02000
K963012 BIOJECT NEEDLE-FREE VIAL ADAPTER (13MM)
K861687 BIOJECTOR SYRINGE SYSTEM