Medical Device Manufacturer · US , Denver , CO

In-X Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - In-X Corp. Anesthesiology ✕

2 devices
1-2 of 2
Cleared Dec 18, 2001
HOME-AWAY SYSTEM
K004047 · CAW
Anesthesiology · 354d
Cleared Aug 30, 2000
MINOLTA PULSOX-3/MINOLTA PULSOX-3I
K984570 · DQA
Anesthesiology · 616d
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