OXY MONITOR 5-RANGE DUAL-THERMISTOR
K-Number: K832652 · 1983-12-22
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Device Summary
Frequently Asked Questions
What is the OXY MONITOR 5-RANGE DUAL-THERMISTOR?
OXY MONITOR 5-RANGE DUAL-THERMISTOR is a medical device that received FDA 510(k) clearance on 1983-12-22. The listed applicant is Litton Medical Electronics. The 510(k) number is K832652.
When did OXY MONITOR 5-RANGE DUAL-THERMISTOR receive FDA 510(k) clearance?
OXY MONITOR 5-RANGE DUAL-THERMISTOR received FDA 510(k) clearance on 1983-12-22, under 510(k) number K832652.
Who is the listed applicant for OXY MONITOR 5-RANGE DUAL-THERMISTOR?
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 OXY MONITOR 5-RANGE DUAL-THERMISTOR?
The FDA product code for OXY MONITOR 5-RANGE DUAL-THERMISTOR is KLK.
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: KLK)
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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