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FDA 510(k)

THREE-CHANNEL STRESS TEST SYSTEM (M633)

K-Number: K760854 · 1976-11-12

ApplicantQuinton, Inc.
Decision Date1976-11-12
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THREE-CHANNEL STRESS TEST SYSTEM (M633) is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760854. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THREE-CHANNEL STRESS TEST SYSTEM (M633)?

THREE-CHANNEL STRESS TEST SYSTEM (M633) is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Quinton, Inc.. The 510(k) number is K760854.

When did THREE-CHANNEL STRESS TEST SYSTEM (M633) receive FDA 510(k) clearance?

THREE-CHANNEL STRESS TEST SYSTEM (M633) received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760854.

Who is the listed applicant for THREE-CHANNEL STRESS TEST SYSTEM (M633)?

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 THREE-CHANNEL STRESS TEST SYSTEM (M633)?

The FDA product code for THREE-CHANNEL STRESS TEST SYSTEM (M633) is DPS.

Related Clinical Trials

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.

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.

View all 164 devices →

Related Devices (Code: DPS)

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.

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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