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FDA 510(k)

KALLESTAD ROTAVIRUS MICROPLATE

K-Number: K915137 · 1992-03-04

ApplicantBio-Rad Laboratories, Inc.
Decision Date1992-03-04
Product CodeLIQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

KALLESTAD ROTAVIRUS MICROPLATE 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 1992-03-04 under 510(k) number K915137. The device is classified under product code LIQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KALLESTAD ROTAVIRUS MICROPLATE?

KALLESTAD ROTAVIRUS MICROPLATE is a medical device that received FDA 510(k) clearance on 1992-03-04. The listed applicant is Bio-Rad Laboratories, Inc.. The 510(k) number is K915137.

When did KALLESTAD ROTAVIRUS MICROPLATE receive FDA 510(k) clearance?

KALLESTAD ROTAVIRUS MICROPLATE received FDA 510(k) clearance on 1992-03-04, under 510(k) number K915137.

Who is the listed applicant for KALLESTAD ROTAVIRUS MICROPLATE?

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 KALLESTAD ROTAVIRUS MICROPLATE?

The FDA product code for KALLESTAD ROTAVIRUS MICROPLATE is LIQ.

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Related Devices (Code: LIQ)

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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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