EYR — Tourniquet, Gastro-Urology Class I

FDA Device Classification

FDA product code EYR covers "Tourniquet, Gastro-Urology", a Class I medical device regulated under 21 CFR 878.5900. Submissions are reviewed by the General, Plastic Surgery panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
EYR
Device Class
Class I
Regulation Number
878.5900
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K802850tecnol new jersey wound careTECNOL O.R. TOURNIQUET COVERJanuary 13, 1981
K792256keithley developmentKEITHLEY CLAMPDecember 6, 1979