Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIQUICHEK CARDIAC MARKERS CONTROL (CAT. NO. 685,686,687,688)

K-Number: K961828 · 1996-06-11

ApplicantBio-Rad
Decision Date1996-06-11
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK CARDIAC MARKERS CONTROL (CAT. NO. 685,686,687,688) is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1996-06-11 under 510(k) number K961828. 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 CARDIAC MARKERS CONTROL (CAT. NO. 685,686,687,688)?

LIQUICHEK CARDIAC MARKERS CONTROL (CAT. NO. 685,686,687,688) is a medical device that received FDA 510(k) clearance on 1996-06-11. The listed applicant is Bio-Rad. The 510(k) number is K961828.

When did LIQUICHEK CARDIAC MARKERS CONTROL (CAT. NO. 685,686,687,688) receive FDA 510(k) clearance?

LIQUICHEK CARDIAC MARKERS CONTROL (CAT. NO. 685,686,687,688) received FDA 510(k) clearance on 1996-06-11, under 510(k) number K961828.

Who is the listed applicant for LIQUICHEK CARDIAC MARKERS CONTROL (CAT. NO. 685,686,687,688)?

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 CARDIAC MARKERS CONTROL (CAT. NO. 685,686,687,688)?

The FDA product code for LIQUICHEK CARDIAC MARKERS CONTROL (CAT. NO. 685,686,687,688) 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K171061MRSASelect IIK122187VRESELECT CULTURE MEDIUMK103684VRESELECT CULTURE MEDIUMK093678PLATELIA ASPERGILLUS EIA MODEL 62793K100589MRSA SELECT - SKIN AND SOFT TISSUE WOUND SPECIMENSK081362PLATELIA LYME IGM

View all 319 devices →

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.

K090940SPOTCHECK BLOOD SPOT CONTROL, ASSAYEDAstoria-Pacific, Inc.K062751MODIFICATION TO QUANTIMETRIX CARDIASURE CARDIAC MARKERQuantimetrix Corp.K030768CLINIQA LIQUID QC CARDIAC MARKER CONTROL LEVELS 1, 2 & 3, TRI-LEVELCliniqa CorporationK030102ADVIA CENTAUR AND ACS:180 LIQUID CARDIAC MARKERS 1, 2, 3Bayer Healthcare, LLCK021498LIQUICHEK CARDIAC MARKERS CONTROL LT LEVEL 1, 2, 3, AND TRILEVELBio-RadK012656LIQUICHEK CARDIAC MARKERS CONTROL LT LEVEL 1,2,3, MODELS 646,647,648Bio-Rad

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.

↑