LRL — Cushion, Hemorrhoid Class U

FDA Device Classification

FDA product code LRL covers "Cushion, Hemorrhoid", a Class U medical device. Submissions are reviewed by the Unknown panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LRL
Device Class
Class U
Regulation Number
Submission Type
Review Panel
GU
Medical Specialty
Unknown
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K072690hemawayHEMAWAY SEATDecember 7, 2007
K932396chi'am intlPERI-COMFORT(TM) SEATING CUSHIONSeptember 30, 1993
K864470health aid productsHEMOREST(TM)June 23, 1987