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FDA 510(k)

MLI SET

K-Number: K952392 · 1995-08-07

Decision Date1995-08-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MLI SET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technologies of Georgia. It received FDA 510(k) clearance on 1995-08-07 under 510(k) number K952392. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MLI SET?

MLI SET is a medical device that received FDA 510(k) clearance on 1995-08-07. The listed applicant is Medical Technologies of Georgia. The 510(k) number is K952392.

When did MLI SET receive FDA 510(k) clearance?

MLI SET received FDA 510(k) clearance on 1995-08-07, under 510(k) number K952392.

Who is the listed applicant for MLI SET?

The FDA 510(k) record lists Medical Technologies of Georgia as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MLI SET?

The FDA product code for MLI SET is FPA.

Other records listing Medical Technologies of Georgia 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.

View all 12 devices →

Related Devices (Code: FPA)

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.

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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