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FDA 510(k)

PACENTRIC CONNECT, TRAVELER AND WEB

K-Number: K100837 · 2010-12-03

ApplicantFimreite Software AS
Decision Date2010-12-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PACENTRIC CONNECT, TRAVELER AND WEB is the device name listed in this FDA 510(k) record. The listed applicant is Fimreite Software AS. It received FDA 510(k) clearance on 2010-12-03 under 510(k) number K100837. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PACENTRIC CONNECT, TRAVELER AND WEB?

PACENTRIC CONNECT, TRAVELER AND WEB is a medical device that received FDA 510(k) clearance on 2010-12-03. The listed applicant is Fimreite Software AS. The 510(k) number is K100837.

When did PACENTRIC CONNECT, TRAVELER AND WEB receive FDA 510(k) clearance?

PACENTRIC CONNECT, TRAVELER AND WEB received FDA 510(k) clearance on 2010-12-03, under 510(k) number K100837.

Who is the listed applicant for PACENTRIC CONNECT, TRAVELER AND WEB?

The FDA 510(k) record lists Fimreite Software AS as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PACENTRIC CONNECT, TRAVELER AND WEB?

The FDA product code for PACENTRIC CONNECT, TRAVELER AND WEB is LLZ.

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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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