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FDA 510(k)

VLC DR MATERIAL

K-Number: K932395 · 1993-08-25

ApplicantDentsply Intl.
Decision Date1993-08-25
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VLC DR MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1993-08-25 under 510(k) number K932395. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VLC DR MATERIAL?

VLC DR MATERIAL is a medical device that received FDA 510(k) clearance on 1993-08-25. The listed applicant is Dentsply Intl.. The 510(k) number is K932395.

When did VLC DR MATERIAL receive FDA 510(k) clearance?

VLC DR MATERIAL received FDA 510(k) clearance on 1993-08-25, under 510(k) number K932395.

Who is the listed applicant for VLC DR MATERIAL?

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

What is the FDA product code for VLC DR MATERIAL?

The FDA product code for VLC DR MATERIAL is EBF.

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Related Devices (Code: EBF)

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

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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