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FDA 510(k)

MODEL Q55XT POWERED TREADMILL

K-Number: K864013 · 1986-11-14

ApplicantQuinton, Inc.
Decision Date1986-11-14
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL Q55XT POWERED TREADMILL is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1986-11-14 under 510(k) number K864013. 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 MODEL Q55XT POWERED TREADMILL?

MODEL Q55XT POWERED TREADMILL is a medical device that received FDA 510(k) clearance on 1986-11-14. The listed applicant is Quinton, Inc.. The 510(k) number is K864013.

When did MODEL Q55XT POWERED TREADMILL receive FDA 510(k) clearance?

MODEL Q55XT POWERED TREADMILL received FDA 510(k) clearance on 1986-11-14, under 510(k) number K864013.

Who is the listed applicant for MODEL Q55XT POWERED TREADMILL?

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 MODEL Q55XT POWERED TREADMILL?

The FDA product code for MODEL Q55XT POWERED TREADMILL is IOL.

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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.

K032038PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601K021906QUINTON Q-CATH, MODEL 000460K003576Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503K001492QUINTON Q-STRESS, MODEL 000483K992908Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)K990866QUINTON MEDTRACK CR PLUS TREADMILL

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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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