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FDA 510(k)

TROPHY RADIOLOGIE RVG PORTABLE RADIOVISIOGRAPHY

K-Number: K950532 · 1995-04-19

Decision Date1995-04-19
Product CodeEAP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TROPHY RADIOLOGIE RVG PORTABLE RADIOVISIOGRAPHY is the device name listed in this FDA 510(k) record. The listed applicant is Trophy Radiologie. It received FDA 510(k) clearance on 1995-04-19 under 510(k) number K950532. The device is classified under product code EAP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROPHY RADIOLOGIE RVG PORTABLE RADIOVISIOGRAPHY?

TROPHY RADIOLOGIE RVG PORTABLE RADIOVISIOGRAPHY is a medical device that received FDA 510(k) clearance on 1995-04-19. The listed applicant is Trophy Radiologie. The 510(k) number is K950532.

When did TROPHY RADIOLOGIE RVG PORTABLE RADIOVISIOGRAPHY receive FDA 510(k) clearance?

TROPHY RADIOLOGIE RVG PORTABLE RADIOVISIOGRAPHY received FDA 510(k) clearance on 1995-04-19, under 510(k) number K950532.

Who is the listed applicant for TROPHY RADIOLOGIE RVG PORTABLE RADIOVISIOGRAPHY?

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

What is the FDA product code for TROPHY RADIOLOGIE RVG PORTABLE RADIOVISIOGRAPHY?

The FDA product code for TROPHY RADIOLOGIE RVG PORTABLE RADIOVISIOGRAPHY is EAP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Trophy Radiologie as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 16 devices →

Related Devices (Code: EAP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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