LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573
K-Number: K002120 · 2000-08-21
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Device Summary
Frequently Asked Questions
What is the LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573?
LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573 is a medical device that received FDA 510(k) clearance on 2000-08-21. The listed applicant is Bio-Rad. The 510(k) number is K002120.
When did LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573 receive FDA 510(k) clearance?
LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573 received FDA 510(k) clearance on 2000-08-21, under 510(k) number K002120.
Who is the listed applicant for LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573?
The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573?
The FDA product code for LIQUICHEK BLOOD GAS CONTROL, MODEL 571, 572, 573 is JJS.
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 Bio-Rad 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: JJS)
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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