Diomed, Ltd.

Diomed, Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 2002, most recent 2007.

Top product codes for Diomed, Ltd.

GEX — General, Plastic Surgery3 devices

Recent clearances by Diomed, Ltd.

K063828 — DIOMED DELTA 25Code GEX·2007-01-25
K051996 — DIOMED DELTA 15, MODEL DELTA 15; DIOMED DELTA 30, MODEL DELTA 30Code GEX·2005-08-18
K012398 — DIOMED 15 DIODE LASERCode GEX·2002-01-22

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