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FDA 510(k)

POWERED TREADMILL

K-Number: K820548 · 1982-03-15

ApplicantOgden Health Products
Decision Date1982-03-15
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POWERED TREADMILL is the device name listed in this FDA 510(k) record. The listed applicant is Ogden Health Products. It received FDA 510(k) clearance on 1982-03-15 under 510(k) number K820548. The device is classified under product code IOL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWERED TREADMILL?

POWERED TREADMILL is a medical device that received FDA 510(k) clearance on 1982-03-15. The listed applicant is Ogden Health Products. The 510(k) number is K820548.

When did POWERED TREADMILL receive FDA 510(k) clearance?

POWERED TREADMILL received FDA 510(k) clearance on 1982-03-15, under 510(k) number K820548.

Who is the listed applicant for POWERED TREADMILL?

The FDA 510(k) record lists Ogden Health Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWERED TREADMILL?

The FDA product code for POWERED TREADMILL is IOL.

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Related Devices (Code: IOL)

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.

K950377PARKER MODEL PEParker Treadmill Co., Inc.K950376PARKER MODEL PMParker Treadmill Co., Inc.K925839TRACKMASTERJas Manufacturing Co., Inc.K930261RTM REHABILITATION TREADMILL, MODEL #945-200Biodan Medical Systems, Ltd.K904556MANSFIELD CARDIAC ASSIST MODEL 940(TM) IABBoston Scientific CorpK913518TA620 TREADMILL CONTROLLERSiemens Burdick, 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.

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