Medical Device Manufacturer · DE , Berlin

Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB

1 submissions · 1 cleared · Since 2003

Total

Cleared

Denied

Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB — FDA 510(k) Submissions

Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB has submitted 1 FDA 510(k) premarket notifications since 2003, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Calibrator, Primary . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

GONOTEC CALIBRATION SOLUTION 300 MOSMOL/KG FOR OSMOMETER

K032608 · JIS Calibrator, Primary · Chemistry

Oct 2003 57d

Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB

Gonotec Gesellschaft Fuer Mess-Und Regeltechnik MB — FDA 510(k) Submissions

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