INFRARED EAR THERMOMETER, MODEL KI-8120
K-Number: K984551 · 2000-01-14
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Device Summary
Frequently Asked Questions
What is the INFRARED EAR THERMOMETER, MODEL KI-8120?
INFRARED EAR THERMOMETER, MODEL KI-8120 is a medical device that received FDA 510(k) clearance on 2000-01-14. The listed applicant is K-Jump Health Co., Ltd.. The 510(k) number is K984551.
When did INFRARED EAR THERMOMETER, MODEL KI-8120 receive FDA 510(k) clearance?
INFRARED EAR THERMOMETER, MODEL KI-8120 received FDA 510(k) clearance on 2000-01-14, under 510(k) number K984551.
Who is the listed applicant for INFRARED EAR THERMOMETER, MODEL KI-8120?
The FDA 510(k) record lists K-Jump Health Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INFRARED EAR THERMOMETER, MODEL KI-8120?
The FDA product code for INFRARED EAR THERMOMETER, MODEL KI-8120 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 K-Jump Health 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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