TOSHIBA DIGITAL CLINICAL THERMOMETER
K-Number: K881909 · 1988-05-26
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Device Summary
Frequently Asked Questions
What is the TOSHIBA DIGITAL CLINICAL THERMOMETER?
TOSHIBA DIGITAL CLINICAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1988-05-26. The listed applicant is Toshiba Glass Co., Ltd.. The 510(k) number is K881909.
When did TOSHIBA DIGITAL CLINICAL THERMOMETER receive FDA 510(k) clearance?
TOSHIBA DIGITAL CLINICAL THERMOMETER received FDA 510(k) clearance on 1988-05-26, under 510(k) number K881909.
Who is the listed applicant for TOSHIBA DIGITAL CLINICAL THERMOMETER?
The FDA 510(k) record lists Toshiba Glass Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TOSHIBA DIGITAL CLINICAL THERMOMETER?
The FDA product code for TOSHIBA 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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