Medical Device Manufacturer · US , Grand Rapids , MI

Metron U.S., Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1997

Recent clearances: METRON QA-IDS I.V. PUMP TESTER, METRON QA-510 SPO2 ANALYZER, QA-40M DEFIBRILLATOR TESTER

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Metron U.S., Inc. Cardiovascular ✕

2 devices

1-2 of 2

Cleared Jul 01, 1997

QA-40M DEFIBRILLATOR TESTER

Cardiovascular · 320d

Cleared Mar 05, 1997

PS-41 6M PATIENT SIMULATOR

Cardiovascular · 202d