MIRROR, NASO-PHARYNX
K-Number: K770054 · 1977-01-18
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Device Summary
Frequently Asked Questions
What is the MIRROR, NASO-PHARYNX?
MIRROR, NASO-PHARYNX is a medical device that received FDA 510(k) clearance on 1977-01-18. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K770054.
When did MIRROR, NASO-PHARYNX receive FDA 510(k) clearance?
MIRROR, NASO-PHARYNX received FDA 510(k) clearance on 1977-01-18, under 510(k) number K770054.
Who is the listed applicant for MIRROR, NASO-PHARYNX?
The FDA 510(k) record lists Welch Allyn, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MIRROR, NASO-PHARYNX?
The FDA product code for MIRROR, NASO-PHARYNX is KAI.
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 Welch Allyn, 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: KAI)
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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