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FDA 510(k)

TROPHYPAN

K-Number: K023346 · 2003-01-03

ApplicantTrophy Radiologie
Decision Date2003-01-03
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TROPHYPAN is the device name listed in this FDA 510(k) record. The listed applicant is Trophy Radiologie. It received FDA 510(k) clearance on 2003-01-03 under 510(k) number K023346. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROPHYPAN?

TROPHYPAN is a medical device that received FDA 510(k) clearance on 2003-01-03. The listed applicant is Trophy Radiologie. The 510(k) number is K023346.

When did TROPHYPAN receive FDA 510(k) clearance?

TROPHYPAN received FDA 510(k) clearance on 2003-01-03, under 510(k) number K023346.

Who is the listed applicant for TROPHYPAN?

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 TROPHYPAN?

The FDA product code for TROPHYPAN is MUH.

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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 2K012514DIGIPAN / DPIK991455ORTHOSLICE OS1000 SERIES; PANORAMIC ORTHOSLICE OS 1000: OS1000, OS1000E PANORAMIC AND CEPHALOMETRIC ORTHOSLICE OS1000C,K991912MODIFICATION TO DIGIPANK961826DIGIPAN

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Related Devices (Code: MUH)

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.

K251793SOTA Cloud Smart Sensor (1.5)Sota Cloud Corp.K252570EzSensor HD, EzSensor UHDQpix Solutions, Inc.K250687Cocoon Solo (DX-7020s)Dexcowin Global, Inc.K251206Digital X-Ray DentiMax Pro Imaging SystemDentimax, Inc.K240040VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)VATECH Co., Ltd.K242778X Sensor (Model: IOS-A15IF, HDI-15DGF)Qpix Solutions, Inc.

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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