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FDA 510(k)

ROCHE REAGENT FOR MAGNESIUM

K-Number: K901758 · 1990-05-23

ApplicantRoche Diagnostic Systems, Inc.
Decision Date1990-05-23
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ROCHE REAGENT FOR MAGNESIUM is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1990-05-23 under 510(k) number K901758. 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 ROCHE REAGENT FOR MAGNESIUM?

ROCHE REAGENT FOR MAGNESIUM is a medical device that received FDA 510(k) clearance on 1990-05-23. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K901758.

When did ROCHE REAGENT FOR MAGNESIUM receive FDA 510(k) clearance?

ROCHE REAGENT FOR MAGNESIUM received FDA 510(k) clearance on 1990-05-23, under 510(k) number K901758.

Who is the listed applicant for ROCHE REAGENT FOR MAGNESIUM?

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

What is the FDA product code for ROCHE REAGENT FOR MAGNESIUM?

The FDA product code for ROCHE REAGENT FOR MAGNESIUM is JGJ.

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Related Devices (Code: JGJ)

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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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