DIGITAL CLINICAL THERMOMETER
K-Number: K820024 · 1982-04-29
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Device Summary
Frequently Asked Questions
What is the DIGITAL CLINICAL THERMOMETER?
DIGITAL CLINICAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1982-04-29. The listed applicant is Faith & Firsts Enterprises Co., Ltd.. The 510(k) number is K820024.
When did DIGITAL CLINICAL THERMOMETER receive FDA 510(k) clearance?
DIGITAL CLINICAL THERMOMETER received FDA 510(k) clearance on 1982-04-29, under 510(k) number K820024.
Who is the listed applicant for DIGITAL CLINICAL THERMOMETER?
The FDA 510(k) record lists Faith & Firsts Enterprises Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGITAL CLINICAL THERMOMETER?
The FDA product code for 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.
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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