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FDA 510(k)

DELUXE MOTORIZED TREADMILL MODEL #FT2300

K-Number: K872639 · 1987-09-18

Decision Date1987-09-18
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DELUXE MOTORIZED TREADMILL MODEL #FT2300 is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1987-09-18 under 510(k) number K872639. 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 DELUXE MOTORIZED TREADMILL MODEL #FT2300?

DELUXE MOTORIZED TREADMILL MODEL #FT2300 is a medical device that received FDA 510(k) clearance on 1987-09-18. The listed applicant is Invacare Corp.. The 510(k) number is K872639.

When did DELUXE MOTORIZED TREADMILL MODEL #FT2300 receive FDA 510(k) clearance?

DELUXE MOTORIZED TREADMILL MODEL #FT2300 received FDA 510(k) clearance on 1987-09-18, under 510(k) number K872639.

Who is the listed applicant for DELUXE MOTORIZED TREADMILL MODEL #FT2300?

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

What is the FDA product code for DELUXE MOTORIZED TREADMILL MODEL #FT2300?

The FDA product code for DELUXE MOTORIZED TREADMILL MODEL #FT2300 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 Invacare Corp. 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.

View all 111 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.

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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