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FDA 510(k)

CONVEX PROBE, PVE-382M

K-Number: K855124 · 1986-03-12

ApplicantToshiba Medical Systems
Decision Date1986-03-12
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CONVEX PROBE, PVE-382M 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 1986-03-12 under 510(k) number K855124. 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 CONVEX PROBE, PVE-382M?

CONVEX PROBE, PVE-382M is a medical device that received FDA 510(k) clearance on 1986-03-12. The listed applicant is Toshiba Medical Systems. The 510(k) number is K855124.

When did CONVEX PROBE, PVE-382M receive FDA 510(k) clearance?

CONVEX PROBE, PVE-382M received FDA 510(k) clearance on 1986-03-12, under 510(k) number K855124.

Who is the listed applicant for CONVEX PROBE, PVE-382M?

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-382M?

The FDA product code for CONVEX PROBE, PVE-382M is IYO.

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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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