CLINICAL ELECTRONIC THERMOMETERS
K-Number: K850244 · 1985-04-04
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Device Summary
Frequently Asked Questions
What is the CLINICAL ELECTRONIC THERMOMETERS?
CLINICAL ELECTRONIC THERMOMETERS is a medical device that received FDA 510(k) clearance on 1985-04-04. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K850244.
When did CLINICAL ELECTRONIC THERMOMETERS receive FDA 510(k) clearance?
CLINICAL ELECTRONIC THERMOMETERS received FDA 510(k) clearance on 1985-04-04, under 510(k) number K850244.
Who is the listed applicant for CLINICAL ELECTRONIC THERMOMETERS?
The FDA 510(k) record lists Sheridan Catheter Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLINICAL ELECTRONIC THERMOMETERS?
The FDA product code for CLINICAL ELECTRONIC THERMOMETERS 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 Sheridan Catheter Corp. 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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