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FDA 510(k)

MAGNESIOMETER

K-Number: K863069 · 1986-12-31

ApplicantJ. D. Assoc.
Decision Date1986-12-31
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAGNESIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is J. D. Assoc.. It received FDA 510(k) clearance on 1986-12-31 under 510(k) number K863069. 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 MAGNESIOMETER?

MAGNESIOMETER is a medical device that received FDA 510(k) clearance on 1986-12-31. The listed applicant is J. D. Assoc.. The 510(k) number is K863069.

When did MAGNESIOMETER receive FDA 510(k) clearance?

MAGNESIOMETER received FDA 510(k) clearance on 1986-12-31, under 510(k) number K863069.

Who is the listed applicant for MAGNESIOMETER?

The FDA 510(k) record lists J. D. Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNESIOMETER?

The FDA product code for MAGNESIOMETER is JGJ.

Related Clinical Trials

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.

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Other records listing J. D. Assoc. 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.

K863103PEG 6,000K863054AST S.C.E. (GOT)K863079CREATINKINETICK863068LDH S.C.E.K863112PROTEINMETERK863053ALT S.C.E. (GPT)

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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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