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FDA 510(k)

QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH

K-Number: K961014 · 1996-07-31

ApplicantQuinton, Inc.
Decision Date1996-07-31
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1996-07-31 under 510(k) number K961014. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH?

QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 1996-07-31. The listed applicant is Quinton, Inc.. The 510(k) number is K961014.

When did QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH receive FDA 510(k) clearance?

QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH received FDA 510(k) clearance on 1996-07-31, under 510(k) number K961014.

Who is the listed applicant for QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH?

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 MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH?

The FDA product code for QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH is LOS.

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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: LOS)

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.

K090895EKG-PLUS II SOFTWAREBionet Co., Ltd.K083749CARDIOVIEW32 REVIEW MODULEQrs Diagnostic, LLCK073376PHILIPS ECG ALGORITHMPhilips Medical SystemsK023034CARDIOTOUCH-3000Bionet Company, Ltd.K011328CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPHBionet Company, Ltd.K993616CARDIO-CARD INTERPRETATION SYSTEM INasiff Assoc., 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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