Class Class II

Konicaminolta DI-X1 (K230906)

K230906 2023-04-25 Special
Home/ Devices/ Konicaminolta DI-X1 (K230906)

Description

Konicaminolta DI-X1 by Konica Minolta, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230906
Clearance Date2023-04-25
Clearance TypeSpecial
Product CodeLLZ
Regulation Number892.2050

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top