TEMPTELLER INFARED EAR THERMOMETERS, MODEL CT-31/31DX/32/32DX
K-Number: K030299 · 2003-02-25
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Device Summary
Frequently Asked Questions
What is the TEMPTELLER INFARED EAR THERMOMETERS, MODEL CT-31/31DX/32/32DX?
TEMPTELLER INFARED EAR THERMOMETERS, MODEL CT-31/31DX/32/32DX is a medical device that received FDA 510(k) clearance on 2003-02-25. The listed applicant is Oriental System Technology, Inc.. The 510(k) number is K030299.
When did TEMPTELLER INFARED EAR THERMOMETERS, MODEL CT-31/31DX/32/32DX receive FDA 510(k) clearance?
TEMPTELLER INFARED EAR THERMOMETERS, MODEL CT-31/31DX/32/32DX received FDA 510(k) clearance on 2003-02-25, under 510(k) number K030299.
Who is the listed applicant for TEMPTELLER INFARED EAR THERMOMETERS, MODEL CT-31/31DX/32/32DX?
The FDA 510(k) record lists Oriental System Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TEMPTELLER INFARED EAR THERMOMETERS, MODEL CT-31/31DX/32/32DX?
The FDA product code for TEMPTELLER INFARED EAR THERMOMETERS, MODEL CT-31/31DX/32/32DX 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 Oriental System Technology, Inc. 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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