POWERED TREADMILL (30/ST)
K-Number: K761041 · 1976-12-09
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Device Summary
Frequently Asked Questions
What is the POWERED TREADMILL (30/ST)?
POWERED TREADMILL (30/ST) is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Physio-Control Corp.. The 510(k) number is K761041.
When did POWERED TREADMILL (30/ST) receive FDA 510(k) clearance?
POWERED TREADMILL (30/ST) received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761041.
Who is the listed applicant for POWERED TREADMILL (30/ST)?
The FDA 510(k) record lists Physio-Control Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWERED TREADMILL (30/ST)?
The FDA product code for POWERED TREADMILL (30/ST) 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 Physio-Control 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: 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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