FDA 510(k)

CMT-1000

K-Number: K942428 · 1995-05-23

Decision Date1995-05-23

Product CodeLIH

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CMT-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Ems, Inc.. It received FDA 510(k) clearance on 1995-05-23 under 510(k) number K942428. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CMT-1000?

CMT-1000 is a medical device that received FDA 510(k) clearance on 1995-05-23. The listed applicant is Ems, Inc.. The 510(k) number is K942428.

When did CMT-1000 receive FDA 510(k) clearance?

CMT-1000 received FDA 510(k) clearance on 1995-05-23, under 510(k) number K942428.

Who is the listed applicant for CMT-1000?

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

What is the FDA product code for CMT-1000?

The FDA product code for CMT-1000 is LIH.

Other records listing Ems, 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.

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Official Source

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