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FDA 510(k)

CONVEX PROBE, PVE-393M

K-Number: K851526 · 1985-09-23

ApplicantToshiba Medical Systems
Decision Date1985-09-23
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CONVEX PROBE, PVE-393M is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems. It received FDA 510(k) clearance on 1985-09-23 under 510(k) number K851526. 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 CONVEX PROBE, PVE-393M?

CONVEX PROBE, PVE-393M is a medical device that received FDA 510(k) clearance on 1985-09-23. The listed applicant is Toshiba Medical Systems. The 510(k) number is K851526.

When did CONVEX PROBE, PVE-393M receive FDA 510(k) clearance?

CONVEX PROBE, PVE-393M received FDA 510(k) clearance on 1985-09-23, under 510(k) number K851526.

Who is the listed applicant for CONVEX PROBE, PVE-393M?

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

What is the FDA product code for CONVEX PROBE, PVE-393M?

The FDA product code for CONVEX PROBE, PVE-393M is ITX.

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Other records listing Toshiba Medical Systems as applicant

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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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