IRR — Bars, Parallel, Powered Class I

FDA Device Classification

FDA product code IRR covers "Bars, Parallel, Powered", a Class I medical device regulated under 21 CFR 890.5380. Submissions are reviewed by the Physical Medicine panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
IRR
Device Class
Class I
Regulation Number
890.5380
Submission Type
Review Panel
PM
Medical Specialty
Physical Medicine
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K932240bailey mfgMODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARSApril 1, 1994