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FDA 510(k)

CARDIO-EXERCISE TREADMILL 550

K-Number: K771697 · 1977-09-20

ApplicantQuinton, Inc.
Decision Date1977-09-20
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CARDIO-EXERCISE TREADMILL 550 is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1977-09-20 under 510(k) number K771697. 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 CARDIO-EXERCISE TREADMILL 550?

CARDIO-EXERCISE TREADMILL 550 is a medical device that received FDA 510(k) clearance on 1977-09-20. The listed applicant is Quinton, Inc.. The 510(k) number is K771697.

When did CARDIO-EXERCISE TREADMILL 550 receive FDA 510(k) clearance?

CARDIO-EXERCISE TREADMILL 550 received FDA 510(k) clearance on 1977-09-20, under 510(k) number K771697.

Who is the listed applicant for CARDIO-EXERCISE TREADMILL 550?

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 CARDIO-EXERCISE TREADMILL 550?

The FDA product code for CARDIO-EXERCISE TREADMILL 550 is IOL.

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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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