FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

H292 CELL CULTURE

K Number: K960909 · Decision May 30, 1996
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
169
Applicant Total
20
Review Days
86

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Basic Information

Device Name
H292 CELL CULTURE
K Number
K960909
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.2280
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Neogenex
Date Received
March 5, 1996
Decision Date
May 30, 1996
Product Code
KIR
Advisory Committee
Hematology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
KIR Cells, Animal And Human, Cultured

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Other Clearances by Neogenex

K Number Device Name
K965047 MINK LUNG CELL CULTURE
K943887 HUMAN NEWBORN FORESKIN CELL CULTURE
K943888 MDCK CELL CULTURE
K943891 RD CULTURE CELL
K943885 PRIMARY RABBIT KIDNEY CELL CULTURE
K943889 VERO CELL CULTURE
K943886 BGM CELL CULTURE
K943890 WI38 CELL CULTURE
K943884 PRIMARY MONKEY KIDNEY CELL CULTURE
K941714 CHLAMYDIA TRACHOMATIS ANTIGEN TEST
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