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FDA 510(k)

FORA CONTROL SOLUTION, TAIDOC CONTROL SOLUTION

K-Number: K093724 · 2010-07-29

ApplicantTaidoc Technology Corporation
Decision Date2010-07-29
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FORA CONTROL SOLUTION, TAIDOC CONTROL SOLUTION 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 2010-07-29 under 510(k) number K093724. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORA CONTROL SOLUTION, TAIDOC CONTROL SOLUTION?

FORA CONTROL SOLUTION, TAIDOC CONTROL SOLUTION is a medical device that received FDA 510(k) clearance on 2010-07-29. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K093724.

When did FORA CONTROL SOLUTION, TAIDOC CONTROL SOLUTION receive FDA 510(k) clearance?

FORA CONTROL SOLUTION, TAIDOC CONTROL SOLUTION received FDA 510(k) clearance on 2010-07-29, under 510(k) number K093724.

Who is the listed applicant for FORA CONTROL SOLUTION, TAIDOC CONTROL SOLUTION?

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 CONTROL SOLUTION, TAIDOC CONTROL SOLUTION?

The FDA product code for FORA CONTROL SOLUTION, TAIDOC CONTROL SOLUTION is JJX.

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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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