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FDA 510(k)

CSNP-001A NEURO PACKAGE

K-Number: K072693 · 2007-11-01

ApplicantToshiba America Medical Systems, In.C
Decision Date2007-11-01
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CSNP-001A NEURO PACKAGE is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba America Medical Systems, In.C. It received FDA 510(k) clearance on 2007-11-01 under 510(k) number K072693. 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 CSNP-001A NEURO PACKAGE?

CSNP-001A NEURO PACKAGE is a medical device that received FDA 510(k) clearance on 2007-11-01. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K072693.

When did CSNP-001A NEURO PACKAGE receive FDA 510(k) clearance?

CSNP-001A NEURO PACKAGE received FDA 510(k) clearance on 2007-11-01, under 510(k) number K072693.

Who is the listed applicant for CSNP-001A NEURO PACKAGE?

The FDA 510(k) record lists Toshiba America Medical Systems, In.C as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CSNP-001A NEURO PACKAGE?

The FDA product code for CSNP-001A NEURO PACKAGE 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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