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FDA 510(k)

ELECTROGLOTTOGRAPH

K-Number: K990240 · 1999-03-11

ApplicantKay Elemetrics Corp.
Decision Date1999-03-11
Product CodeKLX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ELECTROGLOTTOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Kay Elemetrics Corp.. It received FDA 510(k) clearance on 1999-03-11 under 510(k) number K990240. 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 1999-03-11. The listed applicant is Kay Elemetrics Corp.. The 510(k) number is K990240.

When did ELECTROGLOTTOGRAPH receive FDA 510(k) clearance?

ELECTROGLOTTOGRAPH received FDA 510(k) clearance on 1999-03-11, under 510(k) number K990240.

Who is the listed applicant for ELECTROGLOTTOGRAPH?

The FDA 510(k) record lists Kay Elemetrics Corp. 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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Other records listing Kay Elemetrics Corp. as applicant

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.

K991738DIGITAL VIDEO RECORDING SYSTEMK9547987100 SWALLOWING WORKSTATIONK9212859105 RIGID TELESCOPIC ENDOSCOPEK921184RLS 9100 RHINO-LARYNGEAL STROBOSCOPE

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.

K901609ELECTROGLOTTOGRAPHGlottal Ent., Inc.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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