ACC-U-THERM TEMPERATURE MONITOR
K-Number: K813468 · 1982-01-07
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Device Summary
Frequently Asked Questions
What is the ACC-U-THERM TEMPERATURE MONITOR?
ACC-U-THERM TEMPERATURE MONITOR is a medical device that received FDA 510(k) clearance on 1982-01-07. The listed applicant is Diatek, Inc.. The 510(k) number is K813468.
When did ACC-U-THERM TEMPERATURE MONITOR receive FDA 510(k) clearance?
ACC-U-THERM TEMPERATURE MONITOR received FDA 510(k) clearance on 1982-01-07, under 510(k) number K813468.
Who is the listed applicant for ACC-U-THERM TEMPERATURE MONITOR?
The FDA 510(k) record lists Diatek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACC-U-THERM TEMPERATURE MONITOR?
The FDA product code for ACC-U-THERM TEMPERATURE MONITOR 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 Diatek, 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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