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FDA 510(k)

BTE CPM-10

K-Number: K955105 · 1995-12-29

ApplicantBaltimore Therapeutic Equipment Co.
Decision Date1995-12-29
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BTE CPM-10 is the device name listed in this FDA 510(k) record. The listed applicant is Baltimore Therapeutic Equipment Co.. It received FDA 510(k) clearance on 1995-12-29 under 510(k) number K955105. 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 BTE CPM-10?

BTE CPM-10 is a medical device that received FDA 510(k) clearance on 1995-12-29. The listed applicant is Baltimore Therapeutic Equipment Co.. The 510(k) number is K955105.

When did BTE CPM-10 receive FDA 510(k) clearance?

BTE CPM-10 received FDA 510(k) clearance on 1995-12-29, under 510(k) number K955105.

Who is the listed applicant for BTE CPM-10?

The FDA 510(k) record lists Baltimore Therapeutic Equipment Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BTE CPM-10?

The FDA product code for BTE CPM-10 is BXB.

Other records listing Baltimore Therapeutic Equipment Co. 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.

K955106BTE CPM-20K925225THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACKK933611THE BTE WS30K924414THE BTE DYNAMIC LIFTK895881MOTIONSPECTK800007WORK SIMULATOR

View all 7 devices →

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, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K951028HAMEX TWONorthern Orthopaedic Products, Inc.

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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