CLINIQA LIQUID-QC HCG CONTROL LEVEL 1, 2, AND 3
K-Number: K022232 · 2002-08-01
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Device Summary
Frequently Asked Questions
What is the CLINIQA LIQUID-QC HCG CONTROL LEVEL 1, 2, AND 3?
CLINIQA LIQUID-QC HCG CONTROL LEVEL 1, 2, AND 3 is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is Cliniqa Corporation. The 510(k) number is K022232.
When did CLINIQA LIQUID-QC HCG CONTROL LEVEL 1, 2, AND 3 receive FDA 510(k) clearance?
CLINIQA LIQUID-QC HCG CONTROL LEVEL 1, 2, AND 3 received FDA 510(k) clearance on 2002-08-01, under 510(k) number K022232.
Who is the listed applicant for CLINIQA LIQUID-QC HCG CONTROL LEVEL 1, 2, AND 3?
The FDA 510(k) record lists Cliniqa Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLINIQA LIQUID-QC HCG CONTROL LEVEL 1, 2, AND 3?
The FDA product code for CLINIQA LIQUID-QC HCG CONTROL LEVEL 1, 2, AND 3 is JJX.
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 Cliniqa Corporation 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: JJX)
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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