Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 a medical device manufactured by Nasaleze International, Ltd.. It received FDA 510(k) clearance on 2021-03-26 under approval 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. It is manufactured by Nasaleze International, Ltd.. The 510(k) number is K201734.

When was AllerBlock Junior approved by the FDA?

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

What company makes AllerBlock Junior?

AllerBlock Junior is manufactured by Nasaleze International, Ltd..

What is the FDA product code for AllerBlock Junior?

The FDA product code for AllerBlock Junior is NUP.

Other Devices by Nasaleze International, Ltd.

Related Devices (Code: NUP)

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.