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FDA 510(k)

POWERED TREADMILL (30/ST)

K-Number: K761041 · 1976-12-09

Decision Date1976-12-09
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POWERED TREADMILL (30/ST) is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control Corp.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761041. The device is classified under product code IOL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 80 devices →

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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