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FDA 510(k)

ALARM, THERMAL, THERM-ALERT

K-Number: K760683 · 1976-09-27

Decision Date1976-09-27
Product CodeKPD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALARM, THERMAL, THERM-ALERT is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Care, Inc.. It received FDA 510(k) clearance on 1976-09-27 under 510(k) number K760683. The device is classified under product code KPD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 26 devices →

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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