Class Class II

VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464) (K230600)

K230600 2023-04-28 Abbreviated
Home/ Devices/ VERITON CT 300 Series…

Description

VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464) by Spectrum Dynamics Medical, Ltd. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230600
Clearance Date2023-04-28
Clearance TypeAbbreviated
Product CodeKPS
Regulation Number892.1200

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top