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FDA 510(k)

ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG

K-Number: K821079 · 1982-05-10

ApplicantMs. Kate Teaney
Decision Date1982-05-10
Product CodeKLX
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG is the device name listed in this FDA 510(k) record. The listed applicant is Ms. Kate Teaney. It received FDA 510(k) clearance on 1982-05-10 under 510(k) number K821079. 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 NAKED EGG BOXED EGG?

ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG is a medical device that received FDA 510(k) clearance on 1982-05-10. The listed applicant is Ms. Kate Teaney. The 510(k) number is K821079.

When did ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG receive FDA 510(k) clearance?

ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG received FDA 510(k) clearance on 1982-05-10, under 510(k) number K821079.

Who is the listed applicant for ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG?

The FDA 510(k) record lists Ms. Kate Teaney as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG?

The FDA product code for ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG 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.K901609ELECTROGLOTTOGRAPHGlottal Ent., Inc.K841832GLOTTAL FREQUENCY ANALYSERTeltec Electronic Equipment AB

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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