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FDA 510(k)

TMX-C1/C2 TRADMILL CONTROLLER ACCESS.

K-Number: K851631 · 1985-07-15

Decision Date1985-07-15
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TMX-C1/C2 TRADMILL CONTROLLER ACCESS. is the device name listed in this FDA 510(k) record. The listed applicant is Eaton Medical Group. It received FDA 510(k) clearance on 1985-07-15 under 510(k) number K851631. 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 TMX-C1/C2 TRADMILL CONTROLLER ACCESS.?

TMX-C1/C2 TRADMILL CONTROLLER ACCESS. is a medical device that received FDA 510(k) clearance on 1985-07-15. The listed applicant is Eaton Medical Group. The 510(k) number is K851631.

When did TMX-C1/C2 TRADMILL CONTROLLER ACCESS. receive FDA 510(k) clearance?

TMX-C1/C2 TRADMILL CONTROLLER ACCESS. received FDA 510(k) clearance on 1985-07-15, under 510(k) number K851631.

Who is the listed applicant for TMX-C1/C2 TRADMILL CONTROLLER ACCESS.?

The FDA 510(k) record lists Eaton Medical Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TMX-C1/C2 TRADMILL CONTROLLER ACCESS.?

The FDA product code for TMX-C1/C2 TRADMILL CONTROLLER ACCESS. 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 Eaton Medical Group 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 15 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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