KF - JA DME
Item designated by FDA as Class III Devices
This modifier is only used if the Federal Drug Administration (FDA) has designated that item as a Class III device.
See the FDA website for more information.
- Local Coverage Determinations (LCDs)
- Automatic External Defibrillators
- Osteogenesis Stimulators LCD
Last Updated Tue, 27 Sep 2022 19:46:34 +0000