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FDA 510(k)

NOZEES NOSTRIL DILATOR

K-Number: K862406 · 1986-09-19

ApplicantNozees Co.
Decision Date1986-09-19
Product CodeLWF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NOZEES NOSTRIL DILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Nozees Co.. It received FDA 510(k) clearance on 1986-09-19 under 510(k) number K862406. The device is classified under product code LWF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOZEES NOSTRIL DILATOR?

NOZEES NOSTRIL DILATOR is a medical device that received FDA 510(k) clearance on 1986-09-19. The listed applicant is Nozees Co.. The 510(k) number is K862406.

When did NOZEES NOSTRIL DILATOR receive FDA 510(k) clearance?

NOZEES NOSTRIL DILATOR received FDA 510(k) clearance on 1986-09-19, under 510(k) number K862406.

Who is the listed applicant for NOZEES NOSTRIL DILATOR?

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

What is the FDA product code for NOZEES NOSTRIL DILATOR?

The FDA product code for NOZEES NOSTRIL DILATOR is LWF.

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Related Devices (Code: LWF)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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