Home / Device Classification / FPS

FPS — Board, Bed Class I

FDA Device Classification

Classification Details

Product Code: FPS
Device Class: Class I
Regulation Number: 880.6070
Submission Type
Review Panel: HO
Medical Specialty: General Hospital
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K780230	biomet	BED BOARD	February 28, 1978