FDA 510(k)

SARNS CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT

K-Number: K952879 · 1996-04-22

Decision Date1996-04-22

Product CodeKFM

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SARNS CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1996-04-22 under 510(k) number K952879. 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 CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT?

SARNS CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT is a medical device that received FDA 510(k) clearance on 1996-04-22. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K952879.

When did SARNS CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT receive FDA 510(k) clearance?

SARNS CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT received FDA 510(k) clearance on 1996-04-22, under 510(k) number K952879.

Who is the listed applicant for SARNS CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT?

The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SARNS CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT?

The FDA product code for SARNS CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT is KFM.

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Related Devices (Code: KFM)

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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.