TMX-70 TREADMILL
K-Number: K851629 · 1985-07-09
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Device Summary
Frequently Asked Questions
What is the TMX-70 TREADMILL?
TMX-70 TREADMILL is a medical device that received FDA 510(k) clearance on 1985-07-09. The listed applicant is Eaton Medical Group. The 510(k) number is K851629.
When did TMX-70 TREADMILL receive FDA 510(k) clearance?
TMX-70 TREADMILL received FDA 510(k) clearance on 1985-07-09, under 510(k) number K851629.
Who is the listed applicant for TMX-70 TREADMILL?
The FDA 510(k) record lists Eaton Medical Group as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TMX-70 TREADMILL?
The FDA product code for TMX-70 TREADMILL is IOL.
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 Eaton Medical Group 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: 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.
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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