FDA 510(k)

ADV400 TOE CPM

K-Number: K930780 · 1994-02-17

Decision Date1994-02-17

Product CodeBXB

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

ADV400 TOE CPM is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Kinetics, Inc.. It received FDA 510(k) clearance on 1994-02-17 under 510(k) number K930780. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADV400 TOE CPM?

ADV400 TOE CPM is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Advanced Kinetics, Inc.. The 510(k) number is K930780.

When did ADV400 TOE CPM receive FDA 510(k) clearance?

ADV400 TOE CPM received FDA 510(k) clearance on 1994-02-17, under 510(k) number K930780.

Who is the listed applicant for ADV400 TOE CPM?

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

What is the FDA product code for ADV400 TOE CPM?

The FDA product code for ADV400 TOE CPM is BXB.

Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLC K952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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.