FDA 510(k)

CMT 1000

K-Number: K852390 · 1985-07-19

Decision Date1985-07-19

Product CodeKQX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

CMT 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Prestigeline, Inc.. It received FDA 510(k) clearance on 1985-07-19 under 510(k) number K852390. The device is classified under product code KQX. It was reviewed by the OR 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 1985-07-19. The listed applicant is Prestigeline, Inc.. The 510(k) number is K852390.

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

CMT 1000 received FDA 510(k) clearance on 1985-07-19, under 510(k) number K852390.

Who is the listed applicant for CMT 1000?

The FDA 510(k) record lists Prestigeline, 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 KQX.

Related Devices (Code: KQX)

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.

K011827ORTELIUS 800Orthoscan , Ltd.K971079INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWAREInterlogics, Inc.K9623773D-SPINESkill Technologies, Inc.K961212SPINAL TOUCHFasstech K954647INCLINOMETERJ-Tech, Inc.K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)Greenleaf Medical Systems, Inc.

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.