Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

THERMOCOMP

K-Number: K801553 · 1980-10-31

ApplicantHospital Financial Corp.
Decision Date1980-10-31
Product CodeIYM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THERMOCOMP is the device name listed in this FDA 510(k) record. The listed applicant is Hospital Financial Corp.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K801553. The device is classified under product code IYM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMOCOMP?

THERMOCOMP is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is Hospital Financial Corp.. The 510(k) number is K801553.

When did THERMOCOMP receive FDA 510(k) clearance?

THERMOCOMP received FDA 510(k) clearance on 1980-10-31, under 510(k) number K801553.

Who is the listed applicant for THERMOCOMP?

The FDA 510(k) record lists Hospital Financial Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERMOCOMP?

The FDA product code for THERMOCOMP is IYM.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: IYM)

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.

K863736FMS MODEL 110Flir Medical SystemsK852950VISITHERMC.D. Regelin & Associates, Inc.K823041JEOL MODEL #JTG-500MJeolK812799DCATSDorex, Inc.K812701ORTHO-THERM INFRARED SENSOROrthion Corp.K800491GRAPHIC STRESS TELETHERMOMETRYGst Laboratories of Ca, Inc.

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.

↑