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FDA 510(k)

DENTA PLUS

K-Number: K883403 · 1988-10-25

Decision Date1988-10-25
Product CodeJER
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTA PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Connoisseurs Products Corp.. It received FDA 510(k) clearance on 1988-10-25 under 510(k) number K883403. The device is classified under product code JER. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTA PLUS?

DENTA PLUS is a medical device that received FDA 510(k) clearance on 1988-10-25. The listed applicant is Connoisseurs Products Corp.. The 510(k) number is K883403.

When did DENTA PLUS receive FDA 510(k) clearance?

DENTA PLUS received FDA 510(k) clearance on 1988-10-25, under 510(k) number K883403.

Who is the listed applicant for DENTA PLUS?

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

What is the FDA product code for DENTA PLUS?

The FDA product code for DENTA PLUS is JER.

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.

Related Devices (Code: JER)

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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