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FDA 510(k)

VIP VICTOR INTERACTIVE PROBE

K-Number: K960245 · 1996-04-04

ApplicantPro-Dentec
Decision Date1996-04-04
Product CodeEIX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VIP VICTOR INTERACTIVE PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Dentec. It received FDA 510(k) clearance on 1996-04-04 under 510(k) number K960245. The device is classified under product code EIX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIP VICTOR INTERACTIVE PROBE?

VIP VICTOR INTERACTIVE PROBE is a medical device that received FDA 510(k) clearance on 1996-04-04. The listed applicant is Pro-Dentec. The 510(k) number is K960245.

When did VIP VICTOR INTERACTIVE PROBE receive FDA 510(k) clearance?

VIP VICTOR INTERACTIVE PROBE received FDA 510(k) clearance on 1996-04-04, under 510(k) number K960245.

Who is the listed applicant for VIP VICTOR INTERACTIVE PROBE?

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

What is the FDA product code for VIP VICTOR INTERACTIVE PROBE?

The FDA product code for VIP VICTOR INTERACTIVE PROBE is EIX.

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 Pro-Dentec 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.

Related Devices (Code: EIX)

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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