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FDA 510(k)

LIQUICHEK ENA CONTROL, EIA SCREEN, MODEL NO. 206

K-Number: K984462 · 1998-12-22

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

Device Summary

LIQUICHEK ENA CONTROL, EIA SCREEN, MODEL NO. 206 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 K984462. The device is classified under product code LLL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK ENA CONTROL, EIA SCREEN, MODEL NO. 206?

LIQUICHEK ENA CONTROL, EIA SCREEN, MODEL NO. 206 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 K984462.

When did LIQUICHEK ENA CONTROL, EIA SCREEN, MODEL NO. 206 receive FDA 510(k) clearance?

LIQUICHEK ENA CONTROL, EIA SCREEN, MODEL NO. 206 received FDA 510(k) clearance on 1998-12-22, under 510(k) number K984462.

Who is the listed applicant for LIQUICHEK ENA CONTROL, EIA SCREEN, MODEL NO. 206?

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 ENA CONTROL, EIA SCREEN, MODEL NO. 206?

The FDA product code for LIQUICHEK ENA CONTROL, EIA SCREEN, MODEL NO. 206 is LLL.

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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: LLL)

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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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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