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FDA 510(k)

CIMPAT

K-Number: K830109 · 1983-03-01

ApplicantNorth Pacific Dental, Inc.
Decision Date1983-03-01
Product CodeEMR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CIMPAT 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 1983-03-01 under 510(k) number K830109. The device is classified under product code EMR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIMPAT?

CIMPAT is a medical device that received FDA 510(k) clearance on 1983-03-01. The listed applicant is North Pacific Dental, Inc.. The 510(k) number is K830109.

When did CIMPAT receive FDA 510(k) clearance?

CIMPAT received FDA 510(k) clearance on 1983-03-01, under 510(k) number K830109.

Who is the listed applicant for CIMPAT?

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 CIMPAT?

The FDA product code for CIMPAT is EMR.

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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.

K830113SEPTOPACKK830111SEPTOCALK830106UNICIDEK830114GUTTA PERCHA POINTSK830117ENDOMETK830105VITATHYL

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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