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FDA 510(k)

70-X/RVG (RADIOVISIOGRAPHY)

K-Number: K881133 · 1989-07-20

ApplicantTrophy Radiologie
Decision Date1989-07-20
Product CodeEHO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

70-X/RVG (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 1989-07-20 under 510(k) number K881133. The device is classified under product code EHO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 70-X/RVG (RADIOVISIOGRAPHY)?

70-X/RVG (RADIOVISIOGRAPHY) is a medical device that received FDA 510(k) clearance on 1989-07-20. The listed applicant is Trophy Radiologie. The 510(k) number is K881133.

When did 70-X/RVG (RADIOVISIOGRAPHY) receive FDA 510(k) clearance?

70-X/RVG (RADIOVISIOGRAPHY) received FDA 510(k) clearance on 1989-07-20, under 510(k) number K881133.

Who is the listed applicant for 70-X/RVG (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 70-X/RVG (RADIOVISIOGRAPHY)?

The FDA product code for 70-X/RVG (RADIOVISIOGRAPHY) is EHO.

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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.

K033690TROPHYPAN AND TROPHYPAN CK033419STV PRO 2K023346TROPHYPANK012514DIGIPAN / DPIK991455ORTHOSLICE OS1000 SERIES; PANORAMIC ORTHOSLICE OS 1000: OS1000, OS1000E PANORAMIC AND CEPHALOMETRIC ORTHOSLICE OS1000C,K991912MODIFICATION TO DIGIPAN

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Related Devices (Code: EHO)

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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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