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FDA 510(k)

KING DIAGNOSTICS MAGNESIUM REAGENT

K-Number: K923927 · 1992-09-30

ApplicantKing Diagnostics, Inc.
Decision Date1992-09-30
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KING DIAGNOSTICS MAGNESIUM REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is King Diagnostics, Inc.. It received FDA 510(k) clearance on 1992-09-30 under 510(k) number K923927. 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 KING DIAGNOSTICS MAGNESIUM REAGENT?

KING DIAGNOSTICS MAGNESIUM REAGENT is a medical device that received FDA 510(k) clearance on 1992-09-30. The listed applicant is King Diagnostics, Inc.. The 510(k) number is K923927.

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

KING DIAGNOSTICS MAGNESIUM REAGENT received FDA 510(k) clearance on 1992-09-30, under 510(k) number K923927.

Who is the listed applicant for KING DIAGNOSTICS MAGNESIUM REAGENT?

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

What is the FDA product code for KING DIAGNOSTICS MAGNESIUM REAGENT?

The FDA product code for KING DIAGNOSTICS MAGNESIUM REAGENT is JGJ.

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Other records listing King 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.

K933329KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENTK931834KING SODIUM/POTASSIUM STANDARD MODIFIEDK931773HDL PRECIPITATING REAGENT (DEXTRAN SULFATE)K931326KING DIAGNOSTICS CK REAGENTK923129KING DIAGNOSTICS GLUCOSE (HK) REAGENTK922969KING DIAGNOSTICS UREA NITROGEN REAGENT

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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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