Medical Device Manufacturer · US , Mchenry , IL

Teltec Electronic Equipment AB

1 submissions · 1 cleared · Since 1984

Total

Cleared

Denied

Teltec Electronic Equipment AB — FDA 510(k) Submissions

Teltec Electronic Equipment AB has submitted 1 FDA 510(k) premarket notifications since 1984, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices

1–1 of 1

GLOTTAL FREQUENCY ANALYSER

K841832 · KLX Electroglottograph · Ear, Nose, Throat

Jul 1984 76d

Teltec Electronic Equipment AB

Teltec Electronic Equipment AB — FDA 510(k) Submissions

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