Q50 MEDICAL TREADMILL
K-Number: K862741 · 1986-07-29
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Device Summary
Frequently Asked Questions
What is the Q50 MEDICAL TREADMILL?
Q50 MEDICAL TREADMILL is a medical device that received FDA 510(k) clearance on 1986-07-29. The listed applicant is Quinton, Inc.. The 510(k) number is K862741.
When did Q50 MEDICAL TREADMILL receive FDA 510(k) clearance?
Q50 MEDICAL TREADMILL received FDA 510(k) clearance on 1986-07-29, under 510(k) number K862741.
Who is the listed applicant for Q50 MEDICAL TREADMILL?
The FDA 510(k) record lists Quinton, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Q50 MEDICAL TREADMILL?
The FDA product code for Q50 MEDICAL 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 Quinton, Inc. 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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