DUTECK DIGITAL CLINICAL THERMOMETER
K-Number: K992327 · 1999-08-18
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Device Summary
Frequently Asked Questions
What is the DUTECK DIGITAL CLINICAL THERMOMETER?
DUTECK DIGITAL CLINICAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1999-08-18. The listed applicant is Duteck Industrial Co., Ltd.. The 510(k) number is K992327.
When did DUTECK DIGITAL CLINICAL THERMOMETER receive FDA 510(k) clearance?
DUTECK DIGITAL CLINICAL THERMOMETER received FDA 510(k) clearance on 1999-08-18, under 510(k) number K992327.
Who is the listed applicant for DUTECK DIGITAL CLINICAL THERMOMETER?
The FDA 510(k) record lists Duteck Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUTECK DIGITAL CLINICAL THERMOMETER?
The FDA product code for DUTECK DIGITAL CLINICAL 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 Duteck Industrial Co., 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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