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FDA 510(k)

BECKMAN LIQUID-STAT MAGNESIUM REAGENT & STANDARD

K-Number: K883967 · 1989-01-27

ApplicantBeckman Instruments, Inc.
Decision Date1989-01-27
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BECKMAN LIQUID-STAT MAGNESIUM REAGENT & STANDARD 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 1989-01-27 under 510(k) number K883967. The device is classified under product code JGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKMAN LIQUID-STAT MAGNESIUM REAGENT & STANDARD?

BECKMAN LIQUID-STAT MAGNESIUM REAGENT & STANDARD is a medical device that received FDA 510(k) clearance on 1989-01-27. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K883967.

When did BECKMAN LIQUID-STAT MAGNESIUM REAGENT & STANDARD receive FDA 510(k) clearance?

BECKMAN LIQUID-STAT MAGNESIUM REAGENT & STANDARD received FDA 510(k) clearance on 1989-01-27, under 510(k) number K883967.

Who is the listed applicant for BECKMAN LIQUID-STAT MAGNESIUM REAGENT & STANDARD?

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 LIQUID-STAT MAGNESIUM REAGENT & STANDARD?

The FDA product code for BECKMAN LIQUID-STAT MAGNESIUM REAGENT & STANDARD is JGJ.

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Other records listing Beckman Instruments, Inc. as applicant

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Related Devices (Code: JGJ)

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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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