Medrad, Inc.

Medrad, Inc. holds 105 FDA 510(k) medical device clearances, first cleared 1976, most recent 2014, with 13 FDA device recalls on record.

Clearances by Medrad, Inc. — page 2

101–105 of 105

K800823 — QUICK FILLCode DXT·1980-04-29
K800613 — ANGIOPLASTY INJECTORCode DXT·1980-04-08
K791959 — POST EXTRA SYSTOLIC POSTENTLATORCode IXO·1980-01-09
K781819 — POST EXTRA SYSTOLIC POTENTIATORCode DQO·1979-01-15
K760944 — ANGIOGRAPHIC GUIDEWIRECode DQX·1976-12-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.