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FDA 510(k)

QUINTON MEDTRACK CR PLUS TREADMILL

K-Number: K990866 · 1999-04-29

ApplicantQuinton, Inc.
Decision Date1999-04-29
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUINTON MEDTRACK CR PLUS 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 1999-04-29 under 510(k) number K990866. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUINTON MEDTRACK CR PLUS TREADMILL?

QUINTON MEDTRACK CR PLUS TREADMILL is a medical device that received FDA 510(k) clearance on 1999-04-29. The listed applicant is Quinton, Inc.. The 510(k) number is K990866.

When did QUINTON MEDTRACK CR PLUS TREADMILL receive FDA 510(k) clearance?

QUINTON MEDTRACK CR PLUS TREADMILL received FDA 510(k) clearance on 1999-04-29, under 510(k) number K990866.

Who is the listed applicant for QUINTON MEDTRACK CR PLUS 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 QUINTON MEDTRACK CR PLUS TREADMILL?

The FDA product code for QUINTON MEDTRACK CR PLUS TREADMILL is ISD.

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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)K971397VIEWCATH 3-D CATHETER PULLBACK

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Related Devices (Code: ISD)

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.

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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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