ALARM, THERMAL, THERM-ALERT
K-Number: K760683 · 1976-09-27
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Device Summary
Frequently Asked Questions
What is the ALARM, THERMAL, THERM-ALERT?
ALARM, THERMAL, THERM-ALERT is a medical device that received FDA 510(k) clearance on 1976-09-27. The listed applicant is Respiratory Care, Inc.. The 510(k) number is K760683.
When did ALARM, THERMAL, THERM-ALERT receive FDA 510(k) clearance?
ALARM, THERMAL, THERM-ALERT received FDA 510(k) clearance on 1976-09-27, under 510(k) number K760683.
Who is the listed applicant for ALARM, THERMAL, THERM-ALERT?
The FDA 510(k) record lists Respiratory Care, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALARM, THERMAL, THERM-ALERT?
The FDA product code for ALARM, THERMAL, THERM-ALERT is KPD.
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 Respiratory Care, 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: KPD)
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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