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FDA 510(k)

DEMAND MAGNESIUM

K-Number: K851657 · 1985-05-10

ApplicantCooper Biomedical, Inc.
Decision Date1985-05-10
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DEMAND MAGNESIUM is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Biomedical, Inc.. It received FDA 510(k) clearance on 1985-05-10 under 510(k) number K851657. 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 DEMAND MAGNESIUM?

DEMAND MAGNESIUM is a medical device that received FDA 510(k) clearance on 1985-05-10. The listed applicant is Cooper Biomedical, Inc.. The 510(k) number is K851657.

When did DEMAND MAGNESIUM receive FDA 510(k) clearance?

DEMAND MAGNESIUM received FDA 510(k) clearance on 1985-05-10, under 510(k) number K851657.

Who is the listed applicant for DEMAND MAGNESIUM?

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

What is the FDA product code for DEMAND MAGNESIUM?

The FDA product code for DEMAND MAGNESIUM is JGJ.

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Other records listing Cooper Biomedical, 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.

K863868IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/ALPHA-1 ANTK864512IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/HUMAN HAPTOK863301DEMAND TOTAL PROTEINK861926WORTHINGTON HDL PRECIPITATING REAGENT SETK854130DEMAND ETHYL ALCOHOLK853949DEMAND ACID PHOSPHATASE 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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