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FDA 510(k)

CSBP-001A BODY PERFUSION SYSTEM

K-Number: K090504 · 2009-03-05

ApplicantToshibamedical Systems Corporation
Decision Date2009-03-05
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CSBP-001A BODY PERFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2009-03-05 under 510(k) number K090504. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CSBP-001A BODY PERFUSION SYSTEM?

CSBP-001A BODY PERFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 2009-03-05. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K090504.

When did CSBP-001A BODY PERFUSION SYSTEM receive FDA 510(k) clearance?

CSBP-001A BODY PERFUSION SYSTEM received FDA 510(k) clearance on 2009-03-05, under 510(k) number K090504.

Who is the listed applicant for CSBP-001A BODY PERFUSION SYSTEM?

The FDA 510(k) record lists Toshibamedical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CSBP-001A BODY PERFUSION SYSTEM?

The FDA product code for CSBP-001A BODY PERFUSION SYSTEM is JAK.

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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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