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FDA 510(k)

TECHNICON CHEM I SYSTEM MAGNESIUM METHOD

K-Number: K903306 · 1990-08-29

ApplicantTechnicon Instruments Corp.
Decision Date1990-08-29
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON CHEM I SYSTEM MAGNESIUM METHOD is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1990-08-29 under 510(k) number K903306. 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 TECHNICON CHEM I SYSTEM MAGNESIUM METHOD?

TECHNICON CHEM I SYSTEM MAGNESIUM METHOD is a medical device that received FDA 510(k) clearance on 1990-08-29. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K903306.

When did TECHNICON CHEM I SYSTEM MAGNESIUM METHOD receive FDA 510(k) clearance?

TECHNICON CHEM I SYSTEM MAGNESIUM METHOD received FDA 510(k) clearance on 1990-08-29, under 510(k) number K903306.

Who is the listed applicant for TECHNICON CHEM I SYSTEM MAGNESIUM METHOD?

The FDA 510(k) record lists Technicon Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TECHNICON CHEM I SYSTEM MAGNESIUM METHOD?

The FDA product code for TECHNICON CHEM I SYSTEM MAGNESIUM METHOD is JGJ.

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Other records listing Technicon Instruments Corp. as applicant

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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.

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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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