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FDA 510(k)

LIQUICHEK RHEUMATOID FACTOR CONTROL

K-Number: K960987 · 1996-06-04

ApplicantBio-Rad
Decision Date1996-06-04
Product CodeDHR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK RHEUMATOID FACTOR CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1996-06-04 under 510(k) number K960987. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK RHEUMATOID FACTOR CONTROL?

LIQUICHEK RHEUMATOID FACTOR CONTROL is a medical device that received FDA 510(k) clearance on 1996-06-04. The listed applicant is Bio-Rad. The 510(k) number is K960987.

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

LIQUICHEK RHEUMATOID FACTOR CONTROL received FDA 510(k) clearance on 1996-06-04, under 510(k) number K960987.

Who is the listed applicant for LIQUICHEK RHEUMATOID FACTOR CONTROL?

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 RHEUMATOID FACTOR CONTROL?

The FDA product code for LIQUICHEK RHEUMATOID FACTOR CONTROL is DHR.

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Related Devices (Code: DHR)

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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