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FDA 510(k)

DUALUME LARYNGEAL EXAMINATION TELESCOPE

K-Number: K790845 · 1979-07-24

Decision Date1979-07-24
Product CodeENZ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DUALUME LARYNGEAL EXAMINATION TELESCOPE is the device name listed in this FDA 510(k) record. The listed applicant is National Medical Technology. It received FDA 510(k) clearance on 1979-07-24 under 510(k) number K790845. The device is classified under product code ENZ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUALUME LARYNGEAL EXAMINATION TELESCOPE?

DUALUME LARYNGEAL EXAMINATION TELESCOPE is a medical device that received FDA 510(k) clearance on 1979-07-24. The listed applicant is National Medical Technology. The 510(k) number is K790845.

When did DUALUME LARYNGEAL EXAMINATION TELESCOPE receive FDA 510(k) clearance?

DUALUME LARYNGEAL EXAMINATION TELESCOPE received FDA 510(k) clearance on 1979-07-24, under 510(k) number K790845.

Who is the listed applicant for DUALUME LARYNGEAL EXAMINATION TELESCOPE?

The FDA 510(k) record lists National Medical Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUALUME LARYNGEAL EXAMINATION TELESCOPE?

The FDA product code for DUALUME LARYNGEAL EXAMINATION TELESCOPE is ENZ.

Related Clinical Trials

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.

Other records listing National Medical Technology 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.

Related Devices (Code: ENZ)

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.

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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