FDA 510(k)

MG

K-Number: K981192 · 1998-05-01

Decision Date1998-05-01

Product CodeJGJ

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

MG is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1998-05-01 under 510(k) number K981192. 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 MG?

MG is a medical device that received FDA 510(k) clearance on 1998-05-01. The listed applicant is Abbott Laboratories. The 510(k) number is K981192.

When did MG receive FDA 510(k) clearance?

MG received FDA 510(k) clearance on 1998-05-01, under 510(k) number K981192.

Who is the listed applicant for MG?

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

What is the FDA product code for MG?

The FDA product code for MG is JGJ.

Other records listing Abbott Laboratories as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.