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

CITOJECT CARTRIDGE SYRINGE

K Number: K842006 · Decision Jul 16, 1984
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
44
Applicant Total
158
Review Days
60

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Basic Information

Device Name
CITOJECT CARTRIDGE SYRINGE
K Number
K842006
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6770
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Miles Laboratories, Inc.
Date Received
May 17, 1984
Decision Date
July 16, 1984
Product Code
EJI
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EJI Syringe, Cartridge

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K871835 GLUCOMETER QC BLOOD METER, AMES GLUCO SYSTEM PRINT
K872120 SERALYZER III BLOOD CHEMISTRY ANALYZER
K873304 CLINITEK AUTO 2000 REAGENT CASSETTE (LEUKOCYTES)
K872634 CUTTER PUREFLO PLUS IV FILTER
K870214 MODIFIED SALTEX REAGENT STRIPS
K870752 SERALYZER LDH/TOTAL BILIRUBIN/TRIGLYCERIDES STRIPS
K865053 SERA-TEK MICROSOMAL ANTIBODY TEST
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