LME TEMP. MONITOR
K-Number: K832042 · 1983-08-12
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Device Summary
Frequently Asked Questions
What is the LME TEMP. MONITOR?
LME TEMP. MONITOR is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Litton Medical Electronics. The 510(k) number is K832042.
When did LME TEMP. MONITOR receive FDA 510(k) clearance?
LME TEMP. MONITOR received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832042.
Who is the listed applicant for LME TEMP. MONITOR?
The FDA 510(k) record lists Litton Medical Electronics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LME TEMP. MONITOR?
The FDA product code for LME TEMP. 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 Litton Medical Electronics 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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