FDA 510(k)

MLT-2

K-Number: K935981 · 1994-02-17

Decision Date1994-02-17

Product CodeILQ

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

MLT-2 is the device name listed in this FDA 510(k) record. The listed applicant is Med Labs, Inc.. It received FDA 510(k) clearance on 1994-02-17 under 510(k) number K935981. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MLT-2?

MLT-2 is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Med Labs, Inc.. The 510(k) number is K935981.

When did MLT-2 receive FDA 510(k) clearance?

MLT-2 received FDA 510(k) clearance on 1994-02-17, under 510(k) number K935981.

Who is the listed applicant for MLT-2?

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

What is the FDA product code for MLT-2?

The FDA product code for MLT-2 is ILQ.

Other records listing Med Labs, Inc. 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.

K960457ELECTRONIC MUSCLE STIMULATOR MODEL EMS-1C/EMS-2C K923819EEC-1 PACKAGE K903652SCAN COM AND SCAN COM P (TENTATIVE)

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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.