DST — Clip, Vena-Cava Class II

FDA Device Classification

FDA product code DST covers "Clip, Vena-Cava", a Class II medical device regulated under 21 CFR 870.3260. Submissions are reviewed by the Cardiovascular panel. Devices under this code are implants. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
DST
Device Class
Class II
Regulation Number
870.3260
Submission Type
Review Panel
CV
Medical Specialty
Cardiovascular
Implant
Yes

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K900207medicompEPICARDIA 4000July 31, 1990