Medical Device Manufacturer · JP , Tokyo

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

2 submissions · 2 cleared · Since 2009
2
Total
2
Cleared
0
Denied

Chest M.I., Inc. has 2 FDA 510(k) cleared medical devices. Based in Tokyo, JP.

Historical record: 2 cleared submissions from 2009 to 2009. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Chest M.I., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Chest M.I., Inc.
2 devices
1-2 of 2
Cleared Jul 23, 2009
CARDIOTECH SPIROMETRY SYSTEM, MODEL GT-105
K090646 · BZG
Anesthesiology · 134d
Cleared Jan 21, 2009
SPIRO-MASTER PC-10 SPIROMETRY SYSTEM
K080921 · BZG
Anesthesiology · 295d
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