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

CORNING 780 FLUOROMETER/DENSITOMETER

K Number: K850617 · Decision Mar 12, 1985
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
17
Applicant Total
111
Review Days
25

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Basic Information

Device Name
CORNING 780 FLUOROMETER/DENSITOMETER
K Number
K850617
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2400
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Corning Medical & Scientific
Date Received
February 15, 1985
Decision Date
March 12, 1985
Product Code
JQT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JQT Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica

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