T600 TREADMILL
K-Number: K910867 · 1991-05-31
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Device Summary
Frequently Asked Questions
What is the T600 TREADMILL?
T600 TREADMILL is a medical device that received FDA 510(k) clearance on 1991-05-31. The listed applicant is Siemens Burdick, Inc.. The 510(k) number is K910867.
When did T600 TREADMILL receive FDA 510(k) clearance?
T600 TREADMILL received FDA 510(k) clearance on 1991-05-31, under 510(k) number K910867.
Who is the listed applicant for T600 TREADMILL?
The FDA 510(k) record lists Siemens Burdick, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T600 TREADMILL?
The FDA product code for T600 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 Siemens Burdick, 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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