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FDA 510(k)

BentrioTM Allergy Blocker

K-Number: K213114 · 2022-06-24

ApplicantAltamira Therapeutics, Inc.
Decision Date2022-06-24
Product CodeNUP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BentrioTM Allergy Blocker is a medical device manufactured by Altamira Therapeutics, Inc.. It received FDA 510(k) clearance on 2022-06-24 under approval number K213114. 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 BentrioTM Allergy Blocker?

BentrioTM Allergy Blocker is a medical device that received FDA 510(k) clearance on 2022-06-24. It is manufactured by Altamira Therapeutics, Inc.. The 510(k) number is K213114.

When was BentrioTM Allergy Blocker approved by the FDA?

BentrioTM Allergy Blocker received FDA 510(k) clearance on 2022-06-24, under approval number K213114.

What company makes BentrioTM Allergy Blocker?

BentrioTM Allergy Blocker is manufactured by Altamira Therapeutics, Inc..

What is the FDA product code for BentrioTM Allergy Blocker?

The FDA product code for BentrioTM 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

Related Devices (Code: NUP)

K170848Alzair Allergy BlockerNasaleze International, Ltd. K201734AllerBlock JuniorNasaleze International, Ltd.

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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