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FDA 510(k)

SERIES 1800 EXERCISE TREADMILL

K-Number: K802836 · 1980-12-11

ApplicantMarquette Electronics, Inc.
Decision Date1980-12-11
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SERIES 1800 EXERCISE TREADMILL is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Electronics, Inc.. It received FDA 510(k) clearance on 1980-12-11 under 510(k) number K802836. 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 SERIES 1800 EXERCISE TREADMILL?

SERIES 1800 EXERCISE TREADMILL is a medical device that received FDA 510(k) clearance on 1980-12-11. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K802836.

When did SERIES 1800 EXERCISE TREADMILL receive FDA 510(k) clearance?

SERIES 1800 EXERCISE TREADMILL received FDA 510(k) clearance on 1980-12-11, under 510(k) number K802836.

Who is the listed applicant for SERIES 1800 EXERCISE TREADMILL?

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

What is the FDA product code for SERIES 1800 EXERCISE TREADMILL?

The FDA product code for SERIES 1800 EXERCISE TREADMILL is IOL.

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Other records listing Marquette Electronics, Inc. as applicant

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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.

K950377PARKER MODEL PEParker Treadmill Co., Inc.K950376PARKER MODEL PMParker Treadmill Co., Inc.K925839TRACKMASTERJas Manufacturing Co., Inc.K930261RTM REHABILITATION TREADMILL, MODEL #945-200Biodan Medical Systems, Ltd.K904556MANSFIELD CARDIAC ASSIST MODEL 940(TM) IABBoston Scientific CorpK913518TA620 TREADMILL CONTROLLERSiemens Burdick, Inc.

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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