Cliq Aspirator
K-Number: K201203 · 2020-09-03
Device Summary
Frequently Asked Questions
What is the Cliq Aspirator?
Cliq Aspirator is a medical device that received FDA 510(k) clearance on 2020-09-03. The listed applicant is Anest Iwata Sparmax Co., Ltd.. The 510(k) number is K201203.
When did Cliq Aspirator receive FDA 510(k) clearance?
Cliq Aspirator received FDA 510(k) clearance on 2020-09-03, under 510(k) number K201203.
Who is the listed applicant for Cliq Aspirator?
The FDA 510(k) record lists Anest Iwata Sparmax Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cliq Aspirator?
The FDA product code for Cliq Aspirator is BTA.
Related Devices (Code: BTA)
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.
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.