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

BIOJECTOR 2000 MODEL 1B02000

K Number: K960373 · Decision Mar 5, 1997
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
52
Applicant Total
9
Review Days
404

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Basic Information

Device Name
BIOJECTOR 2000 MODEL 1B02000
K Number
K960373
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5430
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bioject, Inc.
Date Received
January 26, 1996
Decision Date
March 5, 1997
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
K963012 BIOJECT NEEDLE-FREE VIAL ADAPTER (13MM)
K920631 BIOJECT JET INJECTION SYSTEM
K861687 BIOJECTOR SYRINGE SYSTEM