MODIFIED TYMPANIC & ESOPHAGEAL/RECTAL TEMP. SENSOR
K-Number: K874523 · 1988-01-06
Advertisement
Device Summary
Frequently Asked Questions
What is the MODIFIED TYMPANIC & ESOPHAGEAL/RECTAL TEMP. SENSOR?
MODIFIED TYMPANIC & ESOPHAGEAL/RECTAL TEMP. 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 K874523.
When did MODIFIED TYMPANIC & ESOPHAGEAL/RECTAL TEMP. SENSOR receive FDA 510(k) clearance?
MODIFIED TYMPANIC & ESOPHAGEAL/RECTAL TEMP. SENSOR received FDA 510(k) clearance on 1988-01-06, under 510(k) number K874523.
Who is the listed applicant for MODIFIED TYMPANIC & ESOPHAGEAL/RECTAL 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 MODIFIED TYMPANIC & ESOPHAGEAL/RECTAL TEMP. SENSOR?
The FDA product code for MODIFIED TYMPANIC & ESOPHAGEAL/RECTAL 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.
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.
Advertisement