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FDA 510(k)

LIQUICHEK ANTI-SS-B CONTROL, EIA, MODEL 210

K-Number: K984478 · 1998-12-22

ApplicantBio-Rad
Decision Date1998-12-22
Product CodeLKJ
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK ANTI-SS-B CONTROL, EIA, MODEL 210 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1998-12-22 under 510(k) number K984478. The device is classified under product code LKJ. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK ANTI-SS-B CONTROL, EIA, MODEL 210?

LIQUICHEK ANTI-SS-B CONTROL, EIA, MODEL 210 is a medical device that received FDA 510(k) clearance on 1998-12-22. The listed applicant is Bio-Rad. The 510(k) number is K984478.

When did LIQUICHEK ANTI-SS-B CONTROL, EIA, MODEL 210 receive FDA 510(k) clearance?

LIQUICHEK ANTI-SS-B CONTROL, EIA, MODEL 210 received FDA 510(k) clearance on 1998-12-22, under 510(k) number K984478.

Who is the listed applicant for LIQUICHEK ANTI-SS-B CONTROL, EIA, MODEL 210?

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 ANTI-SS-B CONTROL, EIA, MODEL 210?

The FDA product code for LIQUICHEK ANTI-SS-B CONTROL, EIA, MODEL 210 is LKJ.

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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

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Related Devices (Code: LKJ)

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.

K210902EliA Ro52, EliA Ro60Phadia ABK113610ANA-SCREEN WITH MDSSBio-Rad LaboratoriesK082759ELIA CENP IMMUNOASSAY, ELIA U1RNP IMMUNOASSAY, ELIA SM IMMUNOASSAY, ELIA RO IMMUNOASSAYPhadia US, Inc.K081104AESKULISA ANA HEP-2, REF 30-7115USAesku DiagnosticsK041658BIOPLEX 200 ANA SCREEN ON THE BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM, MODEL BIOPLEX 2200Bio-Rad Laboratories, Inc.K042416ATHENA MULTI-LYTE ANA-II TEST SYSTEMZeus Scientific, Inc.

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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