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FDA 510(k)

MOTORIZED EXERCISER

K-Number: K822212 · 1982-08-31

ApplicantW.R. Mccullin
Decision Date1982-08-31
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOTORIZED EXERCISER is the device name listed in this FDA 510(k) record. The listed applicant is W.R. Mccullin. It received FDA 510(k) clearance on 1982-08-31 under 510(k) number K822212. 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 MOTORIZED EXERCISER?

MOTORIZED EXERCISER is a medical device that received FDA 510(k) clearance on 1982-08-31. The listed applicant is W.R. Mccullin. The 510(k) number is K822212.

When did MOTORIZED EXERCISER receive FDA 510(k) clearance?

MOTORIZED EXERCISER received FDA 510(k) clearance on 1982-08-31, under 510(k) number K822212.

Who is the listed applicant for MOTORIZED EXERCISER?

The FDA 510(k) record lists W.R. Mccullin as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOTORIZED EXERCISER?

The FDA product code for MOTORIZED EXERCISER is BXB.

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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.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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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