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FDA 510(k)

MON-A-THERM SUBCUTANEOUS TEMP. SENSOR

K-Number: K853392 · 1985-11-22

Decision Date1985-11-22
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MON-A-THERM SUBCUTANEOUS TEMP. 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 1985-11-22 under 510(k) number K853392. 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 MON-A-THERM SUBCUTANEOUS TEMP. SENSOR?

MON-A-THERM SUBCUTANEOUS TEMP. SENSOR is a medical device that received FDA 510(k) clearance on 1985-11-22. The listed applicant is Mon-A-Therm, Inc.. The 510(k) number is K853392.

When did MON-A-THERM SUBCUTANEOUS TEMP. SENSOR receive FDA 510(k) clearance?

MON-A-THERM SUBCUTANEOUS TEMP. SENSOR received FDA 510(k) clearance on 1985-11-22, under 510(k) number K853392.

Who is the listed applicant for MON-A-THERM SUBCUTANEOUS TEMP. 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 MON-A-THERM SUBCUTANEOUS TEMP. SENSOR?

The FDA product code for MON-A-THERM SUBCUTANEOUS TEMP. 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

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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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