FDA Data MCP
☰
Docs
Datasets
Pricing
Blog
Account
Statistics
Get API Key
Home
/
Companies
/ Kinetix
Kinetix
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K832401
RESPIROMETER
April 30, 1984
K840459
IMPROVED MOUTHPIECE
February 17, 1984
K833420
KINETIX MOUTHPIECE
January 10, 1984
K833012
INSPIROMETER
November 8, 1983