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FDA 510(k)

PVK-357AT

K-Number: K943303 · 1995-02-03

ApplicantToshiba America Medical Systems, In.C
Decision Date1995-02-03
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PVK-357AT 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 1995-02-03 under 510(k) number K943303. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PVK-357AT?

PVK-357AT is a medical device that received FDA 510(k) clearance on 1995-02-03. The listed applicant is Toshiba America Medical Systems, In.C. The 510(k) number is K943303.

When did PVK-357AT receive FDA 510(k) clearance?

PVK-357AT received FDA 510(k) clearance on 1995-02-03, under 510(k) number K943303.

Who is the listed applicant for PVK-357AT?

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-357AT?

The FDA product code for PVK-357AT is IYO.

Other records listing Toshiba America Medical Systems, In.C as applicant

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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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