MACHIDA NASOPHARYNGO-LARYNGOSCOPE
K-Number: K811943 · 1981-07-28
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Device Summary
Frequently Asked Questions
What is the MACHIDA NASOPHARYNGO-LARYNGOSCOPE?
MACHIDA NASOPHARYNGO-LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1981-07-28. The listed applicant is Machida America, Inc.. The 510(k) number is K811943.
When did MACHIDA NASOPHARYNGO-LARYNGOSCOPE receive FDA 510(k) clearance?
MACHIDA NASOPHARYNGO-LARYNGOSCOPE received FDA 510(k) clearance on 1981-07-28, under 510(k) number K811943.
Who is the listed applicant for MACHIDA NASOPHARYNGO-LARYNGOSCOPE?
The FDA 510(k) record lists Machida America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MACHIDA NASOPHARYNGO-LARYNGOSCOPE?
The FDA product code for MACHIDA NASOPHARYNGO-LARYNGOSCOPE is EQN.
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 Machida America, Inc. 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: EQN)
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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