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FDA 510(k)

MAGNESIUM REAGENT SET

K-Number: K843893 · 1984-10-30

ApplicantLivonia Diagnostics, Inc.
Decision Date1984-10-30
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAGNESIUM REAGENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Livonia Diagnostics, Inc.. It received FDA 510(k) clearance on 1984-10-30 under 510(k) number K843893. 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 MAGNESIUM REAGENT SET?

MAGNESIUM REAGENT SET is a medical device that received FDA 510(k) clearance on 1984-10-30. The listed applicant is Livonia Diagnostics, Inc.. The 510(k) number is K843893.

When did MAGNESIUM REAGENT SET receive FDA 510(k) clearance?

MAGNESIUM REAGENT SET received FDA 510(k) clearance on 1984-10-30, under 510(k) number K843893.

Who is the listed applicant for MAGNESIUM REAGENT SET?

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

What is the FDA product code for MAGNESIUM REAGENT SET?

The FDA product code for MAGNESIUM REAGENT SET is JGJ.

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Other records listing Livonia Diagnostics, 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.

K852161SERUM IRON/VIBC REAGENT SETK844322SGOT REAGENT SETK844283SGPT REAGENT SETK844237ALKALINE PHOSPHATASE REAGENT SETK844156UREA NITROGEN REAGENT SETK844182INORGANIC PHOSPHORUS REAGENT SET

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Related Devices (Code: JGJ)

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.

K181748MagnesiumAbbott LaboratoriesK173294MagnesiumAbbott LaboratoriesK162200Randox RX Daytona Plus Magnesium (MG)Randox Laboratories, Ltd.K162399Atellica CH Magnesium (Mg)Siemens Healthcare Diagnostics, Inc.K122302ACE MAGNESIUM REGENTAlfa Wassermann Diagnostics Technologies, LLCK111915MAGNESIUM ASSAYSekisui Diagnostics P.E.I., Inc.

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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