MRL — Scale, Sponge, Surgical, Electrically-Powered Class I

FDA Device Classification

FDA product code MRL covers "Scale, Sponge, Surgical, Electrically-Powered", a Class I medical device regulated under 21 CFR 880.2740. Submissions are reviewed by the General Hospital panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
MRL
Device Class
Class I
Regulation Number
880.2740
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K964181surgitracSPONGETRACFebruary 26, 1997