Dynatech/Nevada, Inc.

Dynatech/Nevada, Inc. holds 6 FDA 510(k) medical device clearances, first cleared 1990, most recent 1995.

Top product codes for Dynatech/Nevada, Inc.

Recent clearances by Dynatech/Nevada, Inc.

K942546 — CUFFLINK NON-INVASIVE BLOOD PRESSURE ANALYZERCode DXN·1995-01-27
K935817 — MEDSIM 300 PATIENT SIMULATORCode DRT·1994-01-18
K934254 — IMPULSE 3000 DEFIBRILLATOR ANALYZERCode DRL·1993-11-23
K897074 — MODEL 215M PATIENT SIMULATORCode DSI·1990-05-17
K897029 — MODEL ECG100 SIMULATORCode DPS·1990-04-26
K897096 — MODEL 404A I.V. INFUSION PUMP ANALYZERCode FRN·1990-03-15

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