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FDA 510(k)

PVK-720ST ENDOCAVITARY TRANSDUCER

K-Number: K964865 · 1997-03-10

ApplicantToshiba America Medical Systems, In.C
Decision Date1997-03-10
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PVK-720ST ENDOCAVITARY TRANSDUCER 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 1997-03-10 under 510(k) number K964865. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PVK-720ST ENDOCAVITARY TRANSDUCER?

PVK-720ST ENDOCAVITARY TRANSDUCER is a medical device that received FDA 510(k) clearance on 1997-03-10. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K964865.

When did PVK-720ST ENDOCAVITARY TRANSDUCER receive FDA 510(k) clearance?

PVK-720ST ENDOCAVITARY TRANSDUCER received FDA 510(k) clearance on 1997-03-10, under 510(k) number K964865.

Who is the listed applicant for PVK-720ST ENDOCAVITARY TRANSDUCER?

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 PVK-720ST ENDOCAVITARY TRANSDUCER?

The FDA product code for PVK-720ST ENDOCAVITARY TRANSDUCER is ITX.

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Related Devices (Code: ITX)

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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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