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FDA 510(k)

Electric nasal aspirator (HTD2601US)

K-Number: K241202 · 2024-07-01

ApplicantHetaida Technology Co., Ltd.
Decision Date2024-07-01
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Electric nasal aspirator (HTD2601US) is a medical device manufactured by Hetaida Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-07-01 under approval number K241202. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Electric nasal aspirator (HTD2601US)?

Electric nasal aspirator (HTD2601US) is a medical device that received FDA 510(k) clearance on 2024-07-01. It is manufactured by Hetaida Technology Co., Ltd.. The 510(k) number is K241202.

When was Electric nasal aspirator (HTD2601US) approved by the FDA?

Electric nasal aspirator (HTD2601US) received FDA 510(k) clearance on 2024-07-01, under approval number K241202.

What company makes Electric nasal aspirator (HTD2601US)?

Electric nasal aspirator (HTD2601US) is manufactured by Hetaida Technology Co., Ltd..

What is the FDA product code for Electric nasal aspirator (HTD2601US)?

The FDA product code for Electric nasal aspirator (HTD2601US) is BTA.

Related Clinical Trials

NCT06816875 Comparison of the User Experience of Four Nasal Aspirators in Infants COMPLETED

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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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