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FDA 510(k)

Alzair Allergy Blocker

K-Number: K170848 · 2017-06-14

ApplicantNasaleze International, Ltd.
Decision Date2017-06-14
Product CodeNUP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Alzair Allergy Blocker is a medical device manufactured by Nasaleze International, Ltd.. It received FDA 510(k) clearance on 2017-06-14 under approval number K170848. The device is classified under product code NUP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Alzair Allergy Blocker?

Alzair Allergy Blocker is a medical device that received FDA 510(k) clearance on 2017-06-14. It is manufactured by Nasaleze International, Ltd.. The 510(k) number is K170848.

When was Alzair Allergy Blocker approved by the FDA?

Alzair Allergy Blocker received FDA 510(k) clearance on 2017-06-14, under approval number K170848.

What company makes Alzair Allergy Blocker?

Alzair Allergy Blocker is manufactured by Nasaleze International, Ltd..

What is the FDA product code for Alzair Allergy Blocker?

The FDA product code for Alzair Allergy Blocker is NUP.

Related Clinical Trials

NCT07588672 Evaluation of the Efficacy, Safety, and Tolerability of PL-14 Allergy Blocker Compared to Saline Spray in Patients With Seasonal Allergic Rhinitis NOT_YET_RECRUITING

Other Devices by Nasaleze International, Ltd.

K201734AllerBlock Junior

Related Devices (Code: NUP)

K201734AllerBlock JuniorNasaleze International, Ltd. K213114BentrioTM Allergy BlockerAltamira Therapeutics, Inc.

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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