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FDA 510(k)

LUER LOCK TEMPERATURE SENSOR

K-Number: K830552 · 1983-03-17

Decision Date1983-03-17
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LUER LOCK TEMPERATURE SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Mon-A-Therm, Inc.. It received FDA 510(k) clearance on 1983-03-17 under 510(k) number K830552. 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 LUER LOCK TEMPERATURE SENSOR?

LUER LOCK TEMPERATURE SENSOR is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Mon-A-Therm, Inc.. The 510(k) number is K830552.

When did LUER LOCK TEMPERATURE SENSOR receive FDA 510(k) clearance?

LUER LOCK TEMPERATURE SENSOR received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830552.

Who is the listed applicant for LUER LOCK TEMPERATURE SENSOR?

The FDA 510(k) record lists Mon-A-Therm, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LUER LOCK TEMPERATURE SENSOR?

The FDA product code for LUER LOCK TEMPERATURE SENSOR 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 Mon-A-Therm, Inc. 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 17 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.

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