KPW

Device, Beam Limiting, X-Ray, Diagnostic

Product code: KPW
Device name: Device, Beam Limiting, X-Ray, Diagnostic
Device class: Class 2
21 CFR: 21 CFR 892.1610
Medical specialty: Radiology
Marketing pathway: 510(K) Exempt
510(k) clearances (all years, FDA): 16 (all years; only the last 3 years are listed here)

Official FDA classification page: KPW

Classification and pathway per current FDA publications. Data from openFDA (CC0).