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FDA 510(k)

NASAL/PARANASAL ENDOSCOPE

K-Number: K930931 · 1993-05-17

Decision Date1993-05-17
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NASAL/PARANASAL ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Storz Instrument Co.. It received FDA 510(k) clearance on 1993-05-17 under 510(k) number K930931. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NASAL/PARANASAL ENDOSCOPE?

NASAL/PARANASAL ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1993-05-17. The listed applicant is Storz Instrument Co.. The 510(k) number is K930931.

When did NASAL/PARANASAL ENDOSCOPE receive FDA 510(k) clearance?

NASAL/PARANASAL ENDOSCOPE received FDA 510(k) clearance on 1993-05-17, under 510(k) number K930931.

Who is the listed applicant for NASAL/PARANASAL ENDOSCOPE?

The FDA 510(k) record lists Storz Instrument Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NASAL/PARANASAL ENDOSCOPE?

The FDA product code for NASAL/PARANASAL ENDOSCOPE 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 Storz Instrument Co. 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.

View all 101 devices →

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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