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FDA 510(k)

MAGNESIUM

K-Number: K964915 · 1997-03-26

ApplicantDerma Media Lab., Inc.
Decision Date1997-03-26
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAGNESIUM is the device name listed in this FDA 510(k) record. The listed applicant is Derma Media Lab., Inc.. It received FDA 510(k) clearance on 1997-03-26 under 510(k) number K964915. 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?

MAGNESIUM is a medical device that received FDA 510(k) clearance on 1997-03-26. The listed applicant is Derma Media Lab., Inc.. The 510(k) number is K964915.

When did MAGNESIUM receive FDA 510(k) clearance?

MAGNESIUM received FDA 510(k) clearance on 1997-03-26, under 510(k) number K964915.

Who is the listed applicant for MAGNESIUM?

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

What is the FDA product code for MAGNESIUM?

The FDA product code for MAGNESIUM is JGJ.

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Other records listing Derma Media Lab., 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.

K971309UREAK970664GLUCOSE REAGENTK971072CHOLESTEROL REAGENTK971005TRIGLYCERIDESK970867URIC ACID REAGENTK964913IRON REAGENT

View all 18 devices →

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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