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FDA 510(k)

MAGNESIUM PRODUCT NO'S, 112-01, 112-02

K-Number: K991761 · 1999-09-02

ApplicantA.P. Total Care, Inc.
Decision Date1999-09-02
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAGNESIUM PRODUCT NO'S, 112-01, 112-02 is the device name listed in this FDA 510(k) record. The listed applicant is A.P. Total Care, Inc.. It received FDA 510(k) clearance on 1999-09-02 under 510(k) number K991761. 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 PRODUCT NO'S, 112-01, 112-02?

MAGNESIUM PRODUCT NO'S, 112-01, 112-02 is a medical device that received FDA 510(k) clearance on 1999-09-02. The listed applicant is A.P. Total Care, Inc.. The 510(k) number is K991761.

When did MAGNESIUM PRODUCT NO'S, 112-01, 112-02 receive FDA 510(k) clearance?

MAGNESIUM PRODUCT NO'S, 112-01, 112-02 received FDA 510(k) clearance on 1999-09-02, under 510(k) number K991761.

Who is the listed applicant for MAGNESIUM PRODUCT NO'S, 112-01, 112-02?

The FDA 510(k) record lists A.P. Total Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAGNESIUM PRODUCT NO'S, 112-01, 112-02?

The FDA product code for MAGNESIUM PRODUCT NO'S, 112-01, 112-02 is JGJ.

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Other records listing A.P. Total Care, 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.

K991246FRUCTOSAMINE, MODEL FR 106-01K991762ALKALINE PHOPHATASE (ALP), PRODUCT NO'S 118-01, 118-02K991664LDL CHOLESTEROL, PRODUCT NO'S, 124-01, CH102-01K991665HDL CHOLESTEROL, PRODUCT NO'S 124-01, CH102-01K991866BILIRUBIN, TOTAL AND DIRECT, PRODUCT NO, 122-01, 122-02, 122-03, 122-04K991867INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02

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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