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FDA 510(k)

Q4500 STREE TEST MONITOR

K-Number: K910017 · 1991-11-05

ApplicantQuinton, Inc.
Decision Date1991-11-05
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Q4500 STREE TEST MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1991-11-05 under 510(k) number K910017. 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 Q4500 STREE TEST MONITOR?

Q4500 STREE TEST MONITOR is a medical device that received FDA 510(k) clearance on 1991-11-05. The listed applicant is Quinton, Inc.. The 510(k) number is K910017.

When did Q4500 STREE TEST MONITOR receive FDA 510(k) clearance?

Q4500 STREE TEST MONITOR received FDA 510(k) clearance on 1991-11-05, under 510(k) number K910017.

Who is the listed applicant for Q4500 STREE TEST MONITOR?

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 Q4500 STREE TEST MONITOR?

The FDA product code for Q4500 STREE TEST MONITOR is DPS.

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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.

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Related Devices (Code: DPS)

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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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