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FDA 510(k)

LIQUICHEK BNP CONTROL

K-Number: K043584 · 2005-02-08

Decision Date2005-02-08
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK BNP CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad Laboratories, Inc.. It received FDA 510(k) clearance on 2005-02-08 under 510(k) number K043584. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK BNP CONTROL?

LIQUICHEK BNP CONTROL is a medical device that received FDA 510(k) clearance on 2005-02-08. The listed applicant is Bio-Rad Laboratories, Inc.. The 510(k) number is K043584.

When did LIQUICHEK BNP CONTROL receive FDA 510(k) clearance?

LIQUICHEK BNP CONTROL received FDA 510(k) clearance on 2005-02-08, under 510(k) number K043584.

Who is the listed applicant for LIQUICHEK BNP CONTROL?

The FDA 510(k) record lists Bio-Rad Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUICHEK BNP CONTROL?

The FDA product code for LIQUICHEK BNP CONTROL 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 Bio-Rad Laboratories, Inc. 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.

View all 79 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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