510(k) K810619

710 FLUOROMETER/DENSITOMETER by Corning Medical & Scientific — Product Code JQT

K810619 is an FDA 510(k) premarket notification submitted by Corning Medical & Scientific for the device "710 FLUOROMETER/DENSITOMETER". The FDA issued a decision of Substantially Equivalent on March 27, 1981. 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
March 27, 1981
Date Received
March 9, 1981
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