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FDA 510(k)

UNICIDE

K-Number: K830106 · 1983-03-07

ApplicantNorth Pacific Dental, Inc.
Decision Date1983-03-07
Product CodeLFE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNICIDE is the device name listed in this FDA 510(k) record. The listed applicant is North Pacific Dental, Inc.. It received FDA 510(k) clearance on 1983-03-07 under 510(k) number K830106. The device is classified under product code LFE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNICIDE?

UNICIDE is a medical device that received FDA 510(k) clearance on 1983-03-07. The listed applicant is North Pacific Dental, Inc.. The 510(k) number is K830106.

When did UNICIDE receive FDA 510(k) clearance?

UNICIDE received FDA 510(k) clearance on 1983-03-07, under 510(k) number K830106.

Who is the listed applicant for UNICIDE?

The FDA 510(k) record lists North Pacific Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNICIDE?

The FDA product code for UNICIDE is LFE.

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Other records listing North Pacific Dental, Inc. 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.

K830113SEPTOPACKK830111SEPTOCALK830114GUTTA PERCHA POINTSK830117ENDOMETK830109CIMPATK830105VITATHYL

View all 11 devices →

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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