Cliq Aspirator

FDA 510(k) K201203 · Anest Iwata Sparmax Co., Ltd.

Substantially Equivalent

510(k) numberK201203

Submission

Device name
Cliq Aspirator
Applicant
Anest Iwata Sparmax Co., Ltd.
Taipei, TW
Received
May 4, 2020
Decision date
September 3, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

Other 510(k)s with product code BTA

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K260147Electric nasal aspirator (BC026, BC025, BC023, BC028, BC029, BC036)BTA · Traditional Shenzhen Kingboom Technology Co., Ltd.03/13/2026SE
K251450Baby Nasal Aspirator (BN002); Baby Nasal Aspirator (BN006); Baby Nasal Aspirator…BTA · Special Shenzhen Desida Technology Co., Ltd.06/06/2025SE
K244033Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NASA606,NASA608,NASA610)BTA · Traditional Shenzhen Desida Technology Co., Ltd.05/16/2025SE
K251101AIRO Suction Unit (AIRO-01)BTA · Traditional Cro, LLC04/26/2025SE
K250697Electric Nasal Aspirator (BC026, BC025, BC023)BTA · Traditional Shenzhen Kingboom Technology Co., Ltd.04/23/2025SE

Questions and answers

When was Cliq Aspirator cleared by the FDA?

Cliq Aspirator (K201203) received a 510(k) decision of Substantially Equivalent on September 3, 2020, 122 days after the submission was received.

What is the product code of K201203?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.