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FDA 510(k)

THE BLEDSOE PASSIVE MOTION EXERCISER

K-Number: K854354 · 1986-02-06

Decision Date1986-02-06
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE BLEDSOE PASSIVE MOTION EXERCISER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technology and Innovations, Inc.. It received FDA 510(k) clearance on 1986-02-06 under 510(k) number K854354. 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 THE BLEDSOE PASSIVE MOTION EXERCISER?

THE BLEDSOE PASSIVE MOTION EXERCISER is a medical device that received FDA 510(k) clearance on 1986-02-06. The listed applicant is Medical Technology and Innovations, Inc.. The 510(k) number is K854354.

When did THE BLEDSOE PASSIVE MOTION EXERCISER receive FDA 510(k) clearance?

THE BLEDSOE PASSIVE MOTION EXERCISER received FDA 510(k) clearance on 1986-02-06, under 510(k) number K854354.

Who is the listed applicant for THE BLEDSOE PASSIVE MOTION EXERCISER?

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

What is the FDA product code for THE BLEDSOE PASSIVE MOTION EXERCISER?

The FDA product code for THE BLEDSOE PASSIVE MOTION EXERCISER is BXB.

Related Clinical Trials

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.

Other records listing Medical Technology and Innovations, 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.

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.

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.

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