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FDA 510(k)

FORA TD-4245 BLOOD GLUCOSE MONITORING SYSTEM, TD-4245

K-Number: K083664 · 2009-01-09

ApplicantTaidoc Technology Corporation
Decision Date2009-01-09
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FORA TD-4245 BLOOD GLUCOSE MONITORING SYSTEM, TD-4245 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 2009-01-09 under 510(k) number K083664. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORA TD-4245 BLOOD GLUCOSE MONITORING SYSTEM, TD-4245?

FORA TD-4245 BLOOD GLUCOSE MONITORING SYSTEM, TD-4245 is a medical device that received FDA 510(k) clearance on 2009-01-09. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K083664.

When did FORA TD-4245 BLOOD GLUCOSE MONITORING SYSTEM, TD-4245 receive FDA 510(k) clearance?

FORA TD-4245 BLOOD GLUCOSE MONITORING SYSTEM, TD-4245 received FDA 510(k) clearance on 2009-01-09, under 510(k) number K083664.

Who is the listed applicant for FORA TD-4245 BLOOD GLUCOSE MONITORING SYSTEM, TD-4245?

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 TD-4245 BLOOD GLUCOSE MONITORING SYSTEM, TD-4245?

The FDA product code for FORA TD-4245 BLOOD GLUCOSE MONITORING SYSTEM, TD-4245 is CGA.

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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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