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FDA 510(k)

BIOTROL MAGNESIUM CALMAGITE

K-Number: K873180 · 1987-09-02

ApplicantBiotrol, USA, Inc.
Decision Date1987-09-02
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BIOTROL MAGNESIUM CALMAGITE is the device name listed in this FDA 510(k) record. The listed applicant is Biotrol, USA, Inc.. It received FDA 510(k) clearance on 1987-09-02 under 510(k) number K873180. 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 BIOTROL MAGNESIUM CALMAGITE?

BIOTROL MAGNESIUM CALMAGITE is a medical device that received FDA 510(k) clearance on 1987-09-02. The listed applicant is Biotrol, USA, Inc.. The 510(k) number is K873180.

When did BIOTROL MAGNESIUM CALMAGITE receive FDA 510(k) clearance?

BIOTROL MAGNESIUM CALMAGITE received FDA 510(k) clearance on 1987-09-02, under 510(k) number K873180.

Who is the listed applicant for BIOTROL MAGNESIUM CALMAGITE?

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

What is the FDA product code for BIOTROL MAGNESIUM CALMAGITE?

The FDA product code for BIOTROL MAGNESIUM CALMAGITE is 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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