E-CARE INFARED EAR THERMOMETER, MODEL LCT-200
K-Number: K021753 · 2002-08-06
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Device Summary
Frequently Asked Questions
What is the E-CARE INFARED EAR THERMOMETER, MODEL LCT-200?
E-CARE INFARED EAR THERMOMETER, MODEL LCT-200 is a medical device that received FDA 510(k) clearance on 2002-08-06. The listed applicant is E-Care Technology Corporation. The 510(k) number is K021753.
When did E-CARE INFARED EAR THERMOMETER, MODEL LCT-200 receive FDA 510(k) clearance?
E-CARE INFARED EAR THERMOMETER, MODEL LCT-200 received FDA 510(k) clearance on 2002-08-06, under 510(k) number K021753.
Who is the listed applicant for E-CARE INFARED EAR THERMOMETER, MODEL LCT-200?
The FDA 510(k) record lists E-Care Technology Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for E-CARE INFARED EAR THERMOMETER, MODEL LCT-200?
The FDA product code for E-CARE INFARED EAR THERMOMETER, MODEL LCT-200 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 E-Care 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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