DIGITAL CLINICAL THERMOMETER, MODELS ACT 2030, 2038
K-Number: K021612 · 2002-05-30
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Device Summary
Frequently Asked Questions
What is the DIGITAL CLINICAL THERMOMETER, MODELS ACT 2030, 2038?
DIGITAL CLINICAL THERMOMETER, MODELS ACT 2030, 2038 is a medical device that received FDA 510(k) clearance on 2002-05-30. The listed applicant is Actherm, Inc.. The 510(k) number is K021612.
When did DIGITAL CLINICAL THERMOMETER, MODELS ACT 2030, 2038 receive FDA 510(k) clearance?
DIGITAL CLINICAL THERMOMETER, MODELS ACT 2030, 2038 received FDA 510(k) clearance on 2002-05-30, under 510(k) number K021612.
Who is the listed applicant for DIGITAL CLINICAL THERMOMETER, MODELS ACT 2030, 2038?
The FDA 510(k) record lists Actherm, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGITAL CLINICAL THERMOMETER, MODELS ACT 2030, 2038?
The FDA product code for DIGITAL CLINICAL THERMOMETER, MODELS ACT 2030, 2038 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 Actherm, 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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