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FDA 510(k)

ORBITER(TM) TREADMILL

K-Number: K897179 · 1990-02-15

ApplicantLee-Meredith Industries, Inc.
Decision Date1990-02-15
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ORBITER(TM) TREADMILL is the device name listed in this FDA 510(k) record. The listed applicant is Lee-Meredith Industries, Inc.. It received FDA 510(k) clearance on 1990-02-15 under 510(k) number K897179. 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 ORBITER(TM) TREADMILL?

ORBITER(TM) TREADMILL is a medical device that received FDA 510(k) clearance on 1990-02-15. The listed applicant is Lee-Meredith Industries, Inc.. The 510(k) number is K897179.

When did ORBITER(TM) TREADMILL receive FDA 510(k) clearance?

ORBITER(TM) TREADMILL received FDA 510(k) clearance on 1990-02-15, under 510(k) number K897179.

Who is the listed applicant for ORBITER(TM) TREADMILL?

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

What is the FDA product code for ORBITER(TM) TREADMILL?

The FDA product code for ORBITER(TM) TREADMILL is IOL.

Related Clinical Trials

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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

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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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