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FDA 510(k)

SARNS 9000 WITH CENTRIFUGAL PUMP OPTION

K-Number: K884659 · 1989-01-24

Decision Date1989-01-24
Product CodeKFM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SARNS 9000 WITH CENTRIFUGAL PUMP OPTION 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 1989-01-24 under 510(k) number K884659. The device is classified under product code KFM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SARNS 9000 WITH CENTRIFUGAL PUMP OPTION?

SARNS 9000 WITH CENTRIFUGAL PUMP OPTION is a medical device that received FDA 510(k) clearance on 1989-01-24. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K884659.

When did SARNS 9000 WITH CENTRIFUGAL PUMP OPTION receive FDA 510(k) clearance?

SARNS 9000 WITH CENTRIFUGAL PUMP OPTION received FDA 510(k) clearance on 1989-01-24, under 510(k) number K884659.

Who is the listed applicant for SARNS 9000 WITH CENTRIFUGAL PUMP OPTION?

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 WITH CENTRIFUGAL PUMP OPTION?

The FDA product code for SARNS 9000 WITH CENTRIFUGAL PUMP OPTION is KFM.

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 3M Health Care, Sarns 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 76 devices →

Related Devices (Code: KFM)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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