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FDA 510(k)

MODIFIED Q-SERIES OF TREADMILLS

K-Number: K885062 · 1988-12-27

ApplicantQuinton, Inc.
Decision Date1988-12-27
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODIFIED Q-SERIES OF TREADMILLS is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1988-12-27 under 510(k) number K885062. 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 MODIFIED Q-SERIES OF TREADMILLS?

MODIFIED Q-SERIES OF TREADMILLS is a medical device that received FDA 510(k) clearance on 1988-12-27. The listed applicant is Quinton, Inc.. The 510(k) number is K885062.

When did MODIFIED Q-SERIES OF TREADMILLS receive FDA 510(k) clearance?

MODIFIED Q-SERIES OF TREADMILLS received FDA 510(k) clearance on 1988-12-27, under 510(k) number K885062.

Who is the listed applicant for MODIFIED Q-SERIES OF TREADMILLS?

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 MODIFIED Q-SERIES OF TREADMILLS?

The FDA product code for MODIFIED Q-SERIES OF TREADMILLS is IOL.

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Other records listing Quinton, Inc. as applicant

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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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