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FDA 510(k)

LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3

K-Number: K925151 · 1992-12-17

ApplicantBio-Rad
Decision Date1992-12-17
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1992-12-17 under 510(k) number K925151. The device is classified under product code JJT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3?

LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3 is a medical device that received FDA 510(k) clearance on 1992-12-17. The listed applicant is Bio-Rad. The 510(k) number is K925151.

When did LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3 receive FDA 510(k) clearance?

LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3 received FDA 510(k) clearance on 1992-12-17, under 510(k) number K925151.

Who is the listed applicant for LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3?

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 CK-MB CONTROL LEVELS 1,2, AND3?

The FDA product code for LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3 is JJT.

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.

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Related Devices (Code: JJT)

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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