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FDA 510(k)

FORA POCT S10/TD-4258 BLOOD GLUCOSE MONITORING SYSTEM

K-Number: K092688 · 2011-07-06

Decision Date2011-07-06
Product CodeLFR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FORA POCT S10/TD-4258 BLOOD GLUCOSE MONITORING 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 2011-07-06 under 510(k) number K092688. The device is classified under product code LFR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORA POCT S10/TD-4258 BLOOD GLUCOSE MONITORING SYSTEM?

FORA POCT S10/TD-4258 BLOOD GLUCOSE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2011-07-06. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K092688.

When did FORA POCT S10/TD-4258 BLOOD GLUCOSE MONITORING SYSTEM receive FDA 510(k) clearance?

FORA POCT S10/TD-4258 BLOOD GLUCOSE MONITORING SYSTEM received FDA 510(k) clearance on 2011-07-06, under 510(k) number K092688.

Who is the listed applicant for FORA POCT S10/TD-4258 BLOOD GLUCOSE MONITORING 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 POCT S10/TD-4258 BLOOD GLUCOSE MONITORING SYSTEM?

The FDA product code for FORA POCT S10/TD-4258 BLOOD GLUCOSE MONITORING SYSTEM is LFR.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Taidoc Technology Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 121 devices →

Related Devices (Code: LFR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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