Medical Device Manufacturer · US , Carson City , NV

Dynatech/Nevada, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1990

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dynatech/Nevada, Inc. Cardiovascular ✕

5 devices

1-5 of 5

Cleared Jan 27, 1995

CUFFLINK NON-INVASIVE BLOOD PRESSURE ANALYZER

Cardiovascular · 241d

Cleared Jan 18, 1994

MEDSIM 300 PATIENT SIMULATOR

Cardiovascular · 47d

Cleared Nov 23, 1993

IMPULSE 3000 DEFIBRILLATOR ANALYZER

Cardiovascular · 84d

Cleared May 17, 1990

MODEL 215M PATIENT SIMULATOR

Cardiovascular · 146d

Cleared Apr 26, 1990

MODEL ECG100 SIMULATOR

Cardiovascular · 129d