NASOPHARYNGOSCOPE
K-Number: K934422 · 1994-01-27
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Device Summary
Frequently Asked Questions
What is the NASOPHARYNGOSCOPE?
NASOPHARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Marks & Murase. The 510(k) number is K934422.
When did NASOPHARYNGOSCOPE receive FDA 510(k) clearance?
NASOPHARYNGOSCOPE received FDA 510(k) clearance on 1994-01-27, under 510(k) number K934422.
Who is the listed applicant for NASOPHARYNGOSCOPE?
The FDA 510(k) record lists Marks & Murase as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NASOPHARYNGOSCOPE?
The FDA product code for NASOPHARYNGOSCOPE is EOB.
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 Marks & Murase 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: EOB)
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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