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FDA 510(k)

KALESTAD ANA MICROPLATE EIA

K-Number: K924087 · 1992-11-02

ApplicantBio-Rad Laboratories, Inc.
Decision Date1992-11-02
Product CodeLJM
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

KALESTAD ANA MICROPLATE EIA is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad Laboratories, Inc.. It received FDA 510(k) clearance on 1992-11-02 under 510(k) number K924087. The device is classified under product code LJM. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KALESTAD ANA MICROPLATE EIA?

KALESTAD ANA MICROPLATE EIA is a medical device that received FDA 510(k) clearance on 1992-11-02. The listed applicant is Bio-Rad Laboratories, Inc.. The 510(k) number is K924087.

When did KALESTAD ANA MICROPLATE EIA receive FDA 510(k) clearance?

KALESTAD ANA MICROPLATE EIA received FDA 510(k) clearance on 1992-11-02, under 510(k) number K924087.

Who is the listed applicant for KALESTAD ANA MICROPLATE EIA?

The FDA 510(k) record lists Bio-Rad Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KALESTAD ANA MICROPLATE EIA?

The FDA product code for KALESTAD ANA MICROPLATE EIA is LJM.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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