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FDA 510(k)

V-SUPRA PLUS, ALLOY NO. 5025

K-Number: K993508 · 1999-12-06

Decision Date1999-12-06
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

V-SUPRA PLUS, ALLOY NO. 5025 is the device name listed in this FDA 510(k) record. The listed applicant is Metalor Dental USA Corp.. It received FDA 510(k) clearance on 1999-12-06 under 510(k) number K993508. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-SUPRA PLUS, ALLOY NO. 5025?

V-SUPRA PLUS, ALLOY NO. 5025 is a medical device that received FDA 510(k) clearance on 1999-12-06. The listed applicant is Metalor Dental USA Corp.. The 510(k) number is K993508.

When did V-SUPRA PLUS, ALLOY NO. 5025 receive FDA 510(k) clearance?

V-SUPRA PLUS, ALLOY NO. 5025 received FDA 510(k) clearance on 1999-12-06, under 510(k) number K993508.

Who is the listed applicant for V-SUPRA PLUS, ALLOY NO. 5025?

The FDA 510(k) record lists Metalor Dental USA Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-SUPRA PLUS, ALLOY NO. 5025?

The FDA product code for V-SUPRA PLUS, ALLOY NO. 5025 is EJT.

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 Metalor Dental USA Corp. 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 67 devices →

Related Devices (Code: EJT)

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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