DIGITAL THERMOMTER
K-Number: K122520 · 2013-02-05
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Device Summary
Frequently Asked Questions
What is the DIGITAL THERMOMTER?
DIGITAL THERMOMTER is a medical device that received FDA 510(k) clearance on 2013-02-05. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K122520.
When did DIGITAL THERMOMTER receive FDA 510(k) clearance?
DIGITAL THERMOMTER received FDA 510(k) clearance on 2013-02-05, under 510(k) number K122520.
Who is the listed applicant for DIGITAL THERMOMTER?
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 DIGITAL THERMOMTER?
The FDA product code for DIGITAL THERMOMTER is FLL.
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.
Related Devices (Code: FLL)
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
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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