Medical Device Manufacturer · US , Mchenry , IL

Gardner Cryogenics

2 submissions · 2 cleared · Since 1977
2
Total
2
Cleared
0
Denied

Gardner Cryogenics — FDA 510(k) Submissions

Gardner Cryogenics has submitted 2 FDA 510(k) premarket notifications since 1977, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Calibrator, Multi-analyte Mixture, Flowmeter, Calibration, Gas . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Chemistry 1 Anesthesiology 1