Medical Device Manufacturer · US , Mchenry , IL

Holter-Hausner Intl. - FDA 510(k) Cleared Devices

42 submissions · 38 cleared · Since 1978
42
Total
38
Cleared
0
Denied

Holter-Hausner Intl. has 38 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 38 cleared submissions from 1978 to 1988. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Holter-Hausner Intl. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Holter-Hausner Intl.
42 devices
1-12 of 42

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