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FDA 510(k)

NOZOVENT, NASAL DILATOR

K-Number: K904290 · 1991-08-20

ApplicantWpm Intl AB Intl Trade & Managemet Consulting
Decision Date1991-08-20
Product CodeLWF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NOZOVENT, NASAL DILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Wpm Intl AB Intl Trade & Managemet Consulting. It received FDA 510(k) clearance on 1991-08-20 under 510(k) number K904290. 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 NOZOVENT, NASAL DILATOR?

NOZOVENT, NASAL DILATOR is a medical device that received FDA 510(k) clearance on 1991-08-20. The listed applicant is Wpm Intl AB Intl Trade & Managemet Consulting. The 510(k) number is K904290.

When did NOZOVENT, NASAL DILATOR receive FDA 510(k) clearance?

NOZOVENT, NASAL DILATOR received FDA 510(k) clearance on 1991-08-20, under 510(k) number K904290.

Who is the listed applicant for NOZOVENT, NASAL DILATOR?

The FDA 510(k) record lists Wpm Intl AB Intl Trade & Managemet Consulting as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOZOVENT, NASAL DILATOR?

The FDA product code for NOZOVENT, NASAL 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.

K181219OptiPillows EPAP MaskCpapnea Medical SupplyK120665INVENT SNORING DEVICEVentus Medical, Inc.K040491CHIN-UP STRIPDale Miller, Inc. - the Chin-Up CompanyK982929MAXAIR NASAL DILATOR SYSTEMHnl TechnologiesK963326BREATHE FITCambridge Assoc.K962400AIR MAX EXTERNAL NASAL DILATOR STRIPAmerican White Cross, Inc.

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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