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FDA 510(k)

MAGNESIUM REAGENT SET

K-Number: K855190 · 1986-02-18

ApplicantTechnostics Intl.
Decision Date1986-02-18
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAGNESIUM REAGENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Technostics Intl.. It received FDA 510(k) clearance on 1986-02-18 under 510(k) number K855190. 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 REAGENT SET?

MAGNESIUM REAGENT SET is a medical device that received FDA 510(k) clearance on 1986-02-18. The listed applicant is Technostics Intl.. The 510(k) number is K855190.

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

MAGNESIUM REAGENT SET received FDA 510(k) clearance on 1986-02-18, under 510(k) number K855190.

Who is the listed applicant for MAGNESIUM REAGENT SET?

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

What is the FDA product code for MAGNESIUM REAGENT SET?

The FDA product code for MAGNESIUM REAGENT SET is JGJ.

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Other records listing Technostics Intl. 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.

K855188CPK (UV) REAGENT KITK860111URIC ACID REAGENT SETK860110GLUTAMIC PYRUVIC TRANSAMINASE, GPT(UV) REAGENT SETK860109ENZYMATIC UREA NITROGEN REAGENT SETK860112TOTAL LIPIDS REAGENT SETK855185GLUCOSE REAGENT SET

View all 21 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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