CLIQ DV-300 ASPIRATOR
K-Number: K132308 · 2013-12-30
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Device Summary
Frequently Asked Questions
What is the CLIQ DV-300 ASPIRATOR?
CLIQ DV-300 ASPIRATOR is a medical device that received FDA 510(k) clearance on 2013-12-30. The listed applicant is Ding Hwa Co., Ltd.. The 510(k) number is K132308.
When did CLIQ DV-300 ASPIRATOR receive FDA 510(k) clearance?
CLIQ DV-300 ASPIRATOR received FDA 510(k) clearance on 2013-12-30, under 510(k) number K132308.
Who is the listed applicant for CLIQ DV-300 ASPIRATOR?
The FDA 510(k) record lists Ding Hwa Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLIQ DV-300 ASPIRATOR?
The FDA product code for CLIQ DV-300 ASPIRATOR is JCX.
Related Clinical Trials
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.
Other records listing Ding Hwa Co., Ltd. as applicant
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.
Related Devices (Code: JCX)
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.
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