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FDA 510(k)

BECKMAN VALPROIC ACID REAGENT

K-Number: K922844 · 1992-10-26

Decision Date1992-10-26
Product CodeLEG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

BECKMAN VALPROIC ACID 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 1992-10-26 under 510(k) number K922844. The device is classified under product code LEG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKMAN VALPROIC ACID REAGENT?

BECKMAN VALPROIC ACID REAGENT is a medical device that received FDA 510(k) clearance on 1992-10-26. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K922844.

When did BECKMAN VALPROIC ACID REAGENT receive FDA 510(k) clearance?

BECKMAN VALPROIC ACID REAGENT received FDA 510(k) clearance on 1992-10-26, under 510(k) number K922844.

Who is the listed applicant for BECKMAN VALPROIC ACID 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 BECKMAN VALPROIC ACID REAGENT?

The FDA product code for BECKMAN VALPROIC ACID REAGENT is LEG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Beckman Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 281 devices →

Related Devices (Code: LEG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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