STRESS TEST SYSTEM
K-Number: K780166 · 1978-02-21
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Device Summary
Frequently Asked Questions
What is the STRESS TEST SYSTEM?
STRESS TEST SYSTEM is a medical device that received FDA 510(k) clearance on 1978-02-21. The listed applicant is Quinton, Inc.. The 510(k) number is K780166.
When did STRESS TEST SYSTEM receive FDA 510(k) clearance?
STRESS TEST SYSTEM received FDA 510(k) clearance on 1978-02-21, under 510(k) number K780166.
Who is the listed applicant for STRESS TEST SYSTEM?
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 STRESS TEST SYSTEM?
The FDA product code for STRESS TEST SYSTEM 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.
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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