Medical Device Manufacturer · JP , Tokyo

Chest M.I., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009

Recent clearances: CARDIOTECH SPIROMETRY SYSTEM, MODEL GT-105, SPIRO-MASTER PC-10 SPIROMETRY SYSTEM

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Chest M.I., Inc. Anesthesiology ✕

2 devices

1-2 of 2

Cleared Jul 23, 2009

CARDIOTECH SPIROMETRY SYSTEM, MODEL GT-105

Anesthesiology · 134d

Cleared Jan 21, 2009

SPIRO-MASTER PC-10 SPIROMETRY SYSTEM

Anesthesiology · 295d