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FDA 510(k)

LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108

K-Number: K024217 · 2003-01-15

ApplicantBio-Rad
Decision Date2003-01-15
Product CodeDHN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 2003-01-15 under 510(k) number K024217. The device is classified under product code DHN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108?

LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108 is a medical device that received FDA 510(k) clearance on 2003-01-15. The listed applicant is Bio-Rad. The 510(k) number is K024217.

When did LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108 receive FDA 510(k) clearance?

LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108 received FDA 510(k) clearance on 2003-01-15, under 510(k) number K024217.

Who is the listed applicant for LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108?

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 ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108?

The FDA product code for LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108 is DHN.

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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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