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FDA 510(k)

SARNS 9000 HEART-LUNG CONSOLE

K-Number: K871131 · 1987-05-21

Applicant3M Health Care, Sarns
Decision Date1987-05-21
Product CodeDTQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SARNS 9000 HEART-LUNG CONSOLE is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Sarns. It received FDA 510(k) clearance on 1987-05-21 under 510(k) number K871131. The device is classified under product code DTQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SARNS 9000 HEART-LUNG CONSOLE?

SARNS 9000 HEART-LUNG CONSOLE is a medical device that received FDA 510(k) clearance on 1987-05-21. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K871131.

When did SARNS 9000 HEART-LUNG CONSOLE receive FDA 510(k) clearance?

SARNS 9000 HEART-LUNG CONSOLE received FDA 510(k) clearance on 1987-05-21, under 510(k) number K871131.

Who is the listed applicant for SARNS 9000 HEART-LUNG CONSOLE?

The FDA 510(k) record lists 3M Health Care, Sarns as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SARNS 9000 HEART-LUNG CONSOLE?

The FDA product code for SARNS 9000 HEART-LUNG CONSOLE is DTQ.

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Other records listing 3M Health Care, Sarns as applicant

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Related Devices (Code: DTQ)

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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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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