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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 the device name listed in this FDA 510(k) record. The listed applicant is Altamira Therapeutics, Inc.. It received FDA 510(k) clearance on 2022-06-24 under 510(k) 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. The listed applicant is Altamira Therapeutics, Inc.. The 510(k) number is K213114.

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

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

Who is the listed applicant for BentrioTM Allergy Blocker?

The FDA 510(k) record lists Altamira Therapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BentrioTM Allergy Blocker?

The FDA product code for BentrioTM Allergy Blocker is NUP.

Related Devices (Code: NUP)

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 JuniorNasaleze International, Ltd.K170848Alzair Allergy BlockerNasaleze 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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