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FDA 510(k)

TA620 TREADMILL CONTROLLER

K-Number: K913518 · 1991-10-24

Decision Date1991-10-24
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TA620 TREADMILL CONTROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Burdick, Inc.. It received FDA 510(k) clearance on 1991-10-24 under 510(k) number K913518. 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 TA620 TREADMILL CONTROLLER?

TA620 TREADMILL CONTROLLER is a medical device that received FDA 510(k) clearance on 1991-10-24. The listed applicant is Siemens Burdick, Inc.. The 510(k) number is K913518.

When did TA620 TREADMILL CONTROLLER receive FDA 510(k) clearance?

TA620 TREADMILL CONTROLLER received FDA 510(k) clearance on 1991-10-24, under 510(k) number K913518.

Who is the listed applicant for TA620 TREADMILL CONTROLLER?

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 TA620 TREADMILL CONTROLLER?

The FDA product code for TA620 TREADMILL CONTROLLER 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.

View all 7 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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