DUALUME LARYNGEAL EXAMINATION TELESCOPE
K-Number: K790845 · 1979-07-24
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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