KINGTECH DIGITAL THERMOMETER
K-Number: K133111 · 2013-12-26
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Device Summary
Frequently Asked Questions
What is the KINGTECH DIGITAL THERMOMETER?
KINGTECH DIGITAL THERMOMETER is a medical device that received FDA 510(k) clearance on 2013-12-26. The listed applicant is Kingtech Enterprise, Ltd.. The 510(k) number is K133111.
When did KINGTECH DIGITAL THERMOMETER receive FDA 510(k) clearance?
KINGTECH DIGITAL THERMOMETER received FDA 510(k) clearance on 2013-12-26, under 510(k) number K133111.
Who is the listed applicant for KINGTECH DIGITAL THERMOMETER?
The FDA 510(k) record lists Kingtech Enterprise, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KINGTECH DIGITAL THERMOMETER?
The FDA product code for KINGTECH DIGITAL THERMOMETER 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 Kingtech Enterprise, Ltd. 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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