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FDA 510(k)

GLOTTAL FREQUENCY ANALYSER

K-Number: K841832 · 1984-07-18

ApplicantTeltec Electronic Equipment AB
Decision Date1984-07-18
Product CodeKLX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

GLOTTAL FREQUENCY ANALYSER is the device name listed in this FDA 510(k) record. The listed applicant is Teltec Electronic Equipment AB. It received FDA 510(k) clearance on 1984-07-18 under 510(k) number K841832. The device is classified under product code KLX. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLOTTAL FREQUENCY ANALYSER?

GLOTTAL FREQUENCY ANALYSER is a medical device that received FDA 510(k) clearance on 1984-07-18. The listed applicant is Teltec Electronic Equipment AB. The 510(k) number is K841832.

When did GLOTTAL FREQUENCY ANALYSER receive FDA 510(k) clearance?

GLOTTAL FREQUENCY ANALYSER received FDA 510(k) clearance on 1984-07-18, under 510(k) number K841832.

Who is the listed applicant for GLOTTAL FREQUENCY ANALYSER?

The FDA 510(k) record lists Teltec Electronic Equipment AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GLOTTAL FREQUENCY ANALYSER?

The FDA product code for GLOTTAL FREQUENCY ANALYSER is KLX.

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Related Devices (Code: KLX)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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