Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LME TEMP. MONITOR

K-Number: K832042 · 1983-08-12

Decision Date1983-08-12
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LME TEMP. MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Litton Medical Electronics. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832042. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 38 devices →

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.

↑