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FDA 510(k)

PROGRAM. TREADMILL CONTROLLER #645

K-Number: K830146 · 1983-02-02

ApplicantQuinton, Inc.
Decision Date1983-02-02
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PROGRAM. TREADMILL CONTROLLER #645 is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1983-02-02 under 510(k) number K830146. 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 PROGRAM. TREADMILL CONTROLLER #645?

PROGRAM. TREADMILL CONTROLLER #645 is a medical device that received FDA 510(k) clearance on 1983-02-02. The listed applicant is Quinton, Inc.. The 510(k) number is K830146.

When did PROGRAM. TREADMILL CONTROLLER #645 receive FDA 510(k) clearance?

PROGRAM. TREADMILL CONTROLLER #645 received FDA 510(k) clearance on 1983-02-02, under 510(k) number K830146.

Who is the listed applicant for PROGRAM. TREADMILL CONTROLLER #645?

The FDA 510(k) record lists Quinton, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROGRAM. TREADMILL CONTROLLER #645?

The FDA product code for PROGRAM. TREADMILL CONTROLLER #645 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 Quinton, 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 164 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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