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Kinetix

FDA Regulatory Profile

Kinetix appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 30, 1984.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K832401RESPIROMETERApril 30, 1984
K840459IMPROVED MOUTHPIECEFebruary 17, 1984
K833420KINETIX MOUTHPIECEJanuary 10, 1984
K833012INSPIROMETERNovember 8, 1983

FDA data resources