510(k) K770026

FLOUROMETER/DENSITOMETER MODEL 720 by Corning Medical & Scientific — Product Code JQT

K770026 is an FDA 510(k) premarket notification submitted by Corning Medical & Scientific for the device "FLOUROMETER/DENSITOMETER MODEL 720". The FDA issued a decision of Substantially Equivalent on January 26, 1977. The device falls under product code JQT (Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica), a Class I device regulated under 21 CFR 862.2400. Corning Medical & Scientific has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 26, 1977
Date Received
January 6, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica
Device Class
Class I
Regulation Number
862.2400
Review Panel
CH
Submission Type