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FDA 510(k)

LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213

K-Number: K984396 · 1998-12-18

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

Device Summary

LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213 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 K984396. The device is classified under product code LRM. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213?

LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213 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 K984396.

When did LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213 receive FDA 510(k) clearance?

LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213 received FDA 510(k) clearance on 1998-12-18, under 510(k) number K984396.

Who is the listed applicant for LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213?

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 ANTI-DSDNA CONTROL, MODEL 213?

The FDA product code for LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213 is LRM.

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Related Devices (Code: LRM)

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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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