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FDA 510(k)

LIQUICHEK ANA CONTROL, SPECKLED PATTERN, MODEL 202

K-Number: K984400 · 1998-12-18

ApplicantBio-Rad
Decision Date1998-12-18
Product CodeDHN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK ANA CONTROL, SPECKLED PATTERN, MODEL 202 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1998-12-18 under 510(k) number K984400. 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, MODEL 202?

LIQUICHEK ANA CONTROL, SPECKLED PATTERN, MODEL 202 is a medical device that received FDA 510(k) clearance on 1998-12-18. The listed applicant is Bio-Rad. The 510(k) number is K984400.

When did LIQUICHEK ANA CONTROL, SPECKLED PATTERN, MODEL 202 receive FDA 510(k) clearance?

LIQUICHEK ANA CONTROL, SPECKLED PATTERN, MODEL 202 received FDA 510(k) clearance on 1998-12-18, under 510(k) number K984400.

Who is the listed applicant for LIQUICHEK ANA CONTROL, SPECKLED PATTERN, MODEL 202?

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, MODEL 202?

The FDA product code for LIQUICHEK ANA CONTROL, SPECKLED PATTERN, MODEL 202 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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