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FDA 510(k)

RSV (RADIOLOGY SYSTEM VISIODENT

K-Number: K031448 · 2003-07-31

ApplicantVisiodent SA
Decision Date2003-07-31
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RSV (RADIOLOGY SYSTEM VISIODENT is the device name listed in this FDA 510(k) record. The listed applicant is Visiodent SA. It received FDA 510(k) clearance on 2003-07-31 under 510(k) number K031448. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RSV (RADIOLOGY SYSTEM VISIODENT?

RSV (RADIOLOGY SYSTEM VISIODENT is a medical device that received FDA 510(k) clearance on 2003-07-31. The listed applicant is Visiodent SA. The 510(k) number is K031448.

When did RSV (RADIOLOGY SYSTEM VISIODENT receive FDA 510(k) clearance?

RSV (RADIOLOGY SYSTEM VISIODENT received FDA 510(k) clearance on 2003-07-31, under 510(k) number K031448.

Who is the listed applicant for RSV (RADIOLOGY SYSTEM VISIODENT?

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

What is the FDA product code for RSV (RADIOLOGY SYSTEM VISIODENT?

The FDA product code for RSV (RADIOLOGY SYSTEM VISIODENT is EHD.

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Related Devices (Code: EHD)

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.

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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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