FDA 510(k)

Alzair Allergy Blocker

K-Number: K170848 · 2017-06-14

Decision Date2017-06-14

Product CodeNUP

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

Alzair Allergy Blocker is the device name listed in this FDA 510(k) record. The listed applicant is Nasaleze International, Ltd.. It received FDA 510(k) clearance on 2017-06-14 under 510(k) 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. The listed applicant is Nasaleze International, Ltd.. The 510(k) number is K170848.

When did Alzair Allergy Blocker receive FDA 510(k) clearance?

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

Who is the listed applicant for Alzair Allergy Blocker?

The FDA 510(k) record lists Nasaleze International, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Alzair Allergy Blocker?

The FDA product code for Alzair Allergy Blocker is NUP.

Other records listing Nasaleze International, Ltd. 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.

K201734AllerBlock Junior

Related Devices (Code: NUP)

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

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.