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FDA 510(k)

ELECTROGLOTTOGRAPH

K-Number: K901609 · 1990-06-28

ApplicantGlottal Ent., Inc.
Decision Date1990-06-28
Product CodeKLX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ELECTROGLOTTOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Glottal Ent., Inc.. It received FDA 510(k) clearance on 1990-06-28 under 510(k) number K901609. 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 ELECTROGLOTTOGRAPH?

ELECTROGLOTTOGRAPH is a medical device that received FDA 510(k) clearance on 1990-06-28. The listed applicant is Glottal Ent., Inc.. The 510(k) number is K901609.

When did ELECTROGLOTTOGRAPH receive FDA 510(k) clearance?

ELECTROGLOTTOGRAPH received FDA 510(k) clearance on 1990-06-28, under 510(k) number K901609.

Who is the listed applicant for ELECTROGLOTTOGRAPH?

The FDA 510(k) record lists Glottal Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROGLOTTOGRAPH?

The FDA product code for ELECTROGLOTTOGRAPH is KLX.

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Related Devices (Code: KLX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K990240ELECTROGLOTTOGRAPHKay Elemetrics Corp.K841832GLOTTAL FREQUENCY ANALYSERTeltec Electronic Equipment ABK821079ELECTROGLOTTOGRAPH NAKED EGG BOXED EGGMs. Kate Teaney

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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