FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE AND ENDOSHEATH
K-Number: K942265 · 1995-12-22
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Device Summary
Frequently Asked Questions
What is the FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE AND ENDOSHEATH?
FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE AND ENDOSHEATH is a medical device that received FDA 510(k) clearance on 1995-12-22. The listed applicant is Vision-Sciences, Inc.. The 510(k) number is K942265.
When did FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE AND ENDOSHEATH receive FDA 510(k) clearance?
FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE AND ENDOSHEATH received FDA 510(k) clearance on 1995-12-22, under 510(k) number K942265.
Who is the listed applicant for FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE AND ENDOSHEATH?
The FDA 510(k) record lists Vision-Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE AND ENDOSHEATH?
The FDA product code for FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE AND ENDOSHEATH 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 Vision-Sciences, 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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