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FDA 510(k)

CARESIDE MG

K-Number: K991717 · 1999-08-10

ApplicantCareside, Inc.
Decision Date1999-08-10
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CARESIDE MG is the device name listed in this FDA 510(k) record. The listed applicant is Careside, Inc.. It received FDA 510(k) clearance on 1999-08-10 under 510(k) number K991717. 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 CARESIDE MG?

CARESIDE MG is a medical device that received FDA 510(k) clearance on 1999-08-10. The listed applicant is Careside, Inc.. The 510(k) number is K991717.

When did CARESIDE MG receive FDA 510(k) clearance?

CARESIDE MG received FDA 510(k) clearance on 1999-08-10, under 510(k) number K991717.

Who is the listed applicant for CARESIDE MG?

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

What is the FDA product code for CARESIDE MG?

The FDA product code for CARESIDE MG is JGJ.

Related Clinical Trials

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Other records listing Careside, 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.

K020484CARESIDE LDHK020486CARESIDE GGTK020487CARESIDE ALTK020488CARESIDE TRGLYCERIDEK002792CARESIDE CHOLINESTERASEK001462CARESIDE HEMOGLOBIN

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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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