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Kinetix
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Medical Device Manufacturer
·
US , Walker , MI
Kinetix - FDA 510(k) Cleared Devices
4 submissions
·
4 cleared
·
Since 1983
View 4 510(k) Devices ↓
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kinetix
Anesthesiology
✕
4
devices
1-4 of 4
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Cleared
Apr 30, 1984
RESPIROMETER
K832401
·
BZG
Anesthesiology
·
285d
Cleared
Feb 17, 1984
IMPROVED MOUTHPIECE
K840459
·
BYP
Anesthesiology
·
15d
Cleared
Jan 10, 1984
KINETIX MOUTHPIECE
K833420
·
BYP
Anesthesiology
·
99d
Cleared
Nov 08, 1983
INSPIROMETER
K833012
·
BWF
Anesthesiology
·
63d
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4
Anesthesiology
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