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FDA 510(k)

HEALTHMASTER- MODEL 8320 MOTORIZED TREADMILL

K-Number: K844779 · 1985-06-28

Decision Date1985-06-28
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HEALTHMASTER- MODEL 8320 MOTORIZED TREADMILL is the device name listed in this FDA 510(k) record. The listed applicant is Roadmaster Corp.. It received FDA 510(k) clearance on 1985-06-28 under 510(k) number K844779. 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 HEALTHMASTER- MODEL 8320 MOTORIZED TREADMILL?

HEALTHMASTER- MODEL 8320 MOTORIZED TREADMILL is a medical device that received FDA 510(k) clearance on 1985-06-28. The listed applicant is Roadmaster Corp.. The 510(k) number is K844779.

When did HEALTHMASTER- MODEL 8320 MOTORIZED TREADMILL receive FDA 510(k) clearance?

HEALTHMASTER- MODEL 8320 MOTORIZED TREADMILL received FDA 510(k) clearance on 1985-06-28, under 510(k) number K844779.

Who is the listed applicant for HEALTHMASTER- MODEL 8320 MOTORIZED TREADMILL?

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

What is the FDA product code for HEALTHMASTER- MODEL 8320 MOTORIZED TREADMILL?

The FDA product code for HEALTHMASTER- MODEL 8320 MOTORIZED TREADMILL 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.

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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