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FDA 510(k)

LIQUICHEK RETICULOCYTE CONTROL (A)

K-Number: K042836 · 2004-11-05

ApplicantBio-Rad
Decision Date2004-11-05
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK RETICULOCYTE CONTROL (A) is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 2004-11-05 under 510(k) number K042836. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK RETICULOCYTE CONTROL (A)?

LIQUICHEK RETICULOCYTE CONTROL (A) is a medical device that received FDA 510(k) clearance on 2004-11-05. The listed applicant is Bio-Rad. The 510(k) number is K042836.

When did LIQUICHEK RETICULOCYTE CONTROL (A) receive FDA 510(k) clearance?

LIQUICHEK RETICULOCYTE CONTROL (A) received FDA 510(k) clearance on 2004-11-05, under 510(k) number K042836.

Who is the listed applicant for LIQUICHEK RETICULOCYTE CONTROL (A)?

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 RETICULOCYTE CONTROL (A)?

The FDA product code for LIQUICHEK RETICULOCYTE CONTROL (A) is JPK.

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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.

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Related Devices (Code: JPK)

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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