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FDA 510(k)

Cliq Aspirator

K-Number: K201203 · 2020-09-03

ApplicantAnest Iwata Sparmax Co., Ltd.
Decision Date2020-09-03
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Cliq Aspirator is a medical device manufactured by Anest Iwata Sparmax Co., Ltd.. It received FDA 510(k) clearance on 2020-09-03 under approval number K201203. 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 Cliq Aspirator?

Cliq Aspirator is a medical device that received FDA 510(k) clearance on 2020-09-03. It is manufactured by Anest Iwata Sparmax Co., Ltd.. The 510(k) number is K201203.

When was Cliq Aspirator approved by the FDA?

Cliq Aspirator received FDA 510(k) clearance on 2020-09-03, under approval number K201203.

What company makes Cliq Aspirator?

Cliq Aspirator is manufactured by Anest Iwata Sparmax Co., Ltd..

What is the FDA product code for Cliq Aspirator?

The FDA product code for Cliq Aspirator is BTA.

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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.

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