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FDA 510(k)

XPER Technology PREMIUM Pro Blood Glucose Monitoring System

K-Number: K221349 · 2024-11-19

ApplicantTaidoc Technology Corporation
Decision Date2024-11-19
Product CodePZI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

XPER Technology PREMIUM Pro 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 2024-11-19 under 510(k) number K221349. The device is classified under product code PZI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XPER Technology PREMIUM Pro Blood Glucose Monitoring System?

XPER Technology PREMIUM Pro Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2024-11-19. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K221349.

When did XPER Technology PREMIUM Pro Blood Glucose Monitoring System receive FDA 510(k) clearance?

XPER Technology PREMIUM Pro Blood Glucose Monitoring System received FDA 510(k) clearance on 2024-11-19, under 510(k) number K221349.

Who is the listed applicant for XPER Technology PREMIUM Pro 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 XPER Technology PREMIUM Pro Blood Glucose Monitoring System?

The FDA product code for XPER Technology PREMIUM Pro Blood Glucose Monitoring System is PZI.

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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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