FDA 510(k)

AllerBlock Junior

K-Number: K201734 · 2021-03-26

Decision Date2021-03-26

Product CodeNUP

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

AllerBlock Junior 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 2021-03-26 under 510(k) number K201734. 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 AllerBlock Junior?

AllerBlock Junior is a medical device that received FDA 510(k) clearance on 2021-03-26. The listed applicant is Nasaleze International, Ltd.. The 510(k) number is K201734.

When did AllerBlock Junior receive FDA 510(k) clearance?

AllerBlock Junior received FDA 510(k) clearance on 2021-03-26, under 510(k) number K201734.

Who is the listed applicant for AllerBlock Junior?

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 AllerBlock Junior?

The FDA product code for AllerBlock Junior 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.

K170848Alzair Allergy Blocker

Related Devices (Code: NUP)

K213114BentrioTM Allergy BlockerAltamira Therapeutics, Inc.K170848Alzair Allergy BlockerNasaleze 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.