TEMPERATURE MODULE, DUAL
K-Number: K781136 · 1978-08-10
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Device Summary
Frequently Asked Questions
What is the TEMPERATURE MODULE, DUAL?
TEMPERATURE MODULE, DUAL is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Cavitron Corp.. The 510(k) number is K781136.
When did TEMPERATURE MODULE, DUAL receive FDA 510(k) clearance?
TEMPERATURE MODULE, DUAL received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781136.
Who is the listed applicant for TEMPERATURE MODULE, DUAL?
The FDA 510(k) record lists Cavitron Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TEMPERATURE MODULE, DUAL?
The FDA product code for TEMPERATURE MODULE, DUAL 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 Cavitron 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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