FDA 510(k)

SEPTOCAL

K-Number: K830111 · 1983-03-24

Decision Date1983-03-24

Product Code

DecisionSubstantially Equivalent

Device Summary

SEPTOCAL 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 1983-03-24 under 510(k) number K830111. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEPTOCAL?

SEPTOCAL is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is North Pacific Dental, Inc.. The 510(k) number is K830111.

When did SEPTOCAL receive FDA 510(k) clearance?

SEPTOCAL received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830111.

Who is the listed applicant for SEPTOCAL?

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

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Other records listing North Pacific Dental, Inc. as applicant

K830113SEPTOPACK K830106UNICIDE K830114GUTTA PERCHA POINTS K830117ENDOMET K830109CIMPAT K830105VITATHYL

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.