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FDA 510(k)

OXY MONITOR 5-RANGE DUAL-THERMISTOR

K-Number: K832652 · 1983-12-22

Decision Date1983-12-22
Product CodeKLK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXY MONITOR 5-RANGE DUAL-THERMISTOR 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 1983-12-22 under 510(k) number K832652. The device is classified under product code KLK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 38 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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