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)

MODEL HEC-7 HEART EVALUATION COMPUTER

K-Number: K802952 · 1981-01-07

ApplicantKluwe Corp.
Decision Date1981-01-07
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL HEC-7 HEART EVALUATION COMPUTER is the device name listed in this FDA 510(k) record. The listed applicant is Kluwe Corp.. It received FDA 510(k) clearance on 1981-01-07 under 510(k) number K802952. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL HEC-7 HEART EVALUATION COMPUTER?

MODEL HEC-7 HEART EVALUATION COMPUTER is a medical device that received FDA 510(k) clearance on 1981-01-07. The listed applicant is Kluwe Corp.. The 510(k) number is K802952.

When did MODEL HEC-7 HEART EVALUATION COMPUTER receive FDA 510(k) clearance?

MODEL HEC-7 HEART EVALUATION COMPUTER received FDA 510(k) clearance on 1981-01-07, under 510(k) number K802952.

Who is the listed applicant for MODEL HEC-7 HEART EVALUATION COMPUTER?

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

What is the FDA product code for MODEL HEC-7 HEART EVALUATION COMPUTER?

The FDA product code for MODEL HEC-7 HEART EVALUATION COMPUTER is DPS.

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: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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.

↑