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Ametek/Thermox Instruments Division

FDA Regulatory Profile

Ametek/Thermox Instruments Division appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 31, 1988.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K874663MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEMMay 31, 1988
K875183LC OXYGEN ANALYZERMarch 29, 1988

FDA data resources