NASO-LARYNGO-PHARYNGOSCOPE
K-Number: K991560 · 1999-07-13
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Device Summary
Frequently Asked Questions
What is the NASO-LARYNGO-PHARYNGOSCOPE?
NASO-LARYNGO-PHARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1999-07-13. The listed applicant is Fiber Imaging Technologies, Inc.. The 510(k) number is K991560.
When did NASO-LARYNGO-PHARYNGOSCOPE receive FDA 510(k) clearance?
NASO-LARYNGO-PHARYNGOSCOPE received FDA 510(k) clearance on 1999-07-13, under 510(k) number K991560.
Who is the listed applicant for NASO-LARYNGO-PHARYNGOSCOPE?
The FDA 510(k) record lists Fiber Imaging Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NASO-LARYNGO-PHARYNGOSCOPE?
The FDA product code for NASO-LARYNGO-PHARYNGOSCOPE 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 Fiber Imaging Technologies, 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: 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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