MODIFIED SUBCUTANEOUS TEMPERATURE SENSOR
K-Number: K874524 · 1988-01-06
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Device Summary
Frequently Asked Questions
What is the MODIFIED SUBCUTANEOUS TEMPERATURE SENSOR?
MODIFIED SUBCUTANEOUS TEMPERATURE SENSOR is a medical device that received FDA 510(k) clearance on 1988-01-06. The listed applicant is Mon-A-Therm, Inc.. The 510(k) number is K874524.
When did MODIFIED SUBCUTANEOUS TEMPERATURE SENSOR receive FDA 510(k) clearance?
MODIFIED SUBCUTANEOUS TEMPERATURE SENSOR received FDA 510(k) clearance on 1988-01-06, under 510(k) number K874524.
Who is the listed applicant for MODIFIED SUBCUTANEOUS 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 MODIFIED SUBCUTANEOUS TEMPERATURE SENSOR?
The FDA product code for MODIFIED SUBCUTANEOUS 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.
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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