TREADMILL E-17
K-Number: K850044 · 1985-04-04
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Device Summary
Frequently Asked Questions
What is the TREADMILL E-17?
TREADMILL E-17 is a medical device that received FDA 510(k) clearance on 1985-04-04. The listed applicant is Del Mar Avionics. The 510(k) number is K850044.
When did TREADMILL E-17 receive FDA 510(k) clearance?
TREADMILL E-17 received FDA 510(k) clearance on 1985-04-04, under 510(k) number K850044.
Who is the listed applicant for TREADMILL E-17?
The FDA 510(k) record lists Del Mar Avionics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TREADMILL E-17?
The FDA product code for TREADMILL E-17 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 Del Mar Avionics 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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