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FDA 510(k)

V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201

K-Number: K101012 · 2010-12-15

ApplicantTaidoc Technology Corporation
Decision Date2010-12-15
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201 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 2010-12-15 under 510(k) number K101012. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201?

V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201 is a medical device that received FDA 510(k) clearance on 2010-12-15. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K101012.

When did V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201 receive FDA 510(k) clearance?

V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201 received FDA 510(k) clearance on 2010-12-15, under 510(k) number K101012.

Who is the listed applicant for V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201?

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 V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201?

The FDA product code for V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201 is DQA.

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Related Devices (Code: DQA)

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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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