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FDA 510(k)

FORA TELEHEALTH SYSTEM

K-Number: K083046 · 2009-01-16

ApplicantTaidoc Technology Corporation
Decision Date2009-01-16
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FORA TELEHEALTH SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Taidoc Technology Corporation. It received FDA 510(k) clearance on 2009-01-16 under 510(k) number K083046. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORA TELEHEALTH SYSTEM?

FORA TELEHEALTH SYSTEM is a medical device that received FDA 510(k) clearance on 2009-01-16. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K083046.

When did FORA TELEHEALTH SYSTEM receive FDA 510(k) clearance?

FORA TELEHEALTH SYSTEM received FDA 510(k) clearance on 2009-01-16, under 510(k) number K083046.

Who is the listed applicant for FORA TELEHEALTH SYSTEM?

The FDA 510(k) record lists Taidoc Technology Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORA TELEHEALTH SYSTEM?

The FDA product code for FORA TELEHEALTH SYSTEM is DRG.

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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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