510(k) K780318

MODULAR SCANNING DENSITOMETER SYS. by Transidyne General Corp. — Product Code JQT

K780318 is an FDA 510(k) premarket notification submitted by Transidyne General Corp. for the device "MODULAR SCANNING DENSITOMETER SYS.". The FDA issued a decision of Substantially Equivalent on April 12, 1978. The device falls under product code JQT (Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica), a Class I device regulated under 21 CFR 862.2400. Transidyne General Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 12, 1978
Date Received
February 24, 1978
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