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

24 CELL WELLS TISSUE CULTURE

K Number: K823747 · Decision Jan 5, 1983
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
0
Applicant Total
111
Review Days
23

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Basic Information

Device Name
24 CELL WELLS TISSUE CULTURE
K Number
K823747
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Corning Medical & Scientific
Date Received
December 13, 1982
Decision Date
January 5, 1983
Product Code
KJG
Advisory Committee
Pathology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
KJG Tube, Tissue Culture

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