DELUXE MOTORIZED TREADMILL MODEL #FT2300
K-Number: K872639 · 1987-09-18
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Device Summary
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.
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
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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