Dynatech/Nevada, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K942546CUFFLINK NON-INVASIVE BLOOD PRESSURE ANALYZERJanuary 27, 1995
K935817MEDSIM 300 PATIENT SIMULATORJanuary 18, 1994
K934254IMPULSE 3000 DEFIBRILLATOR ANALYZERNovember 23, 1993
K897074MODEL 215M PATIENT SIMULATORMay 17, 1990
K897029MODEL ECG100 SIMULATORApril 26, 1990
K897096MODEL 404A I.V. INFUSION PUMP ANALYZERMarch 15, 1990