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FDA 510(k)

LIQUID-STAT LIQUID REAGENT

K-Number: K800457 · 1980-03-20

ApplicantBeckman Instruments, Inc.
Decision Date1980-03-20
Product CodeCHH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUID-STAT LIQUID REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1980-03-20 under 510(k) number K800457. The device is classified under product code CHH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID-STAT LIQUID REAGENT?

LIQUID-STAT LIQUID REAGENT is a medical device that received FDA 510(k) clearance on 1980-03-20. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K800457.

When did LIQUID-STAT LIQUID REAGENT receive FDA 510(k) clearance?

LIQUID-STAT LIQUID REAGENT received FDA 510(k) clearance on 1980-03-20, under 510(k) number K800457.

Who is the listed applicant for LIQUID-STAT LIQUID REAGENT?

The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUID-STAT LIQUID REAGENT?

The FDA product code for LIQUID-STAT LIQUID REAGENT is CHH.

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Other records listing Beckman Instruments, Inc. as applicant

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Related Devices (Code: CHH)

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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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