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

BIOJECTOR SYRINGE SYSTEM

K Number: K861687 · Decision Apr 23, 1987
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
52
Applicant Total
9
Review Days
356

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Basic Information

Device Name
BIOJECTOR SYRINGE SYSTEM
K Number
K861687
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5430
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Bioject, Inc.
Date Received
May 2, 1986
Decision Date
April 23, 1987
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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K960373 BIOJECTOR 2000 MODEL 1B02000
K963012 BIOJECT NEEDLE-FREE VIAL ADAPTER (13MM)
K920631 BIOJECT JET INJECTION SYSTEM