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)

AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30

K-Number: K880615 · 1988-05-13

ApplicantCardiotechnics, Inc.
Decision Date1988-05-13
Product CodeDXH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30 is the device name listed in this FDA 510(k) record. The listed applicant is Cardiotechnics, Inc.. It received FDA 510(k) clearance on 1988-05-13 under 510(k) number K880615. The device is classified under product code DXH. It was reviewed by the CV advisory panel. Product code DXH falls under the category of Hematology, which includes devices for blood cell counting, coagulation testing, and hemoglobin analysis. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30?

AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30 is a medical device that received FDA 510(k) clearance on 1988-05-13. The listed applicant is Cardiotechnics, Inc.. The 510(k) number is K880615.

When did AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30 receive FDA 510(k) clearance?

AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30 received FDA 510(k) clearance on 1988-05-13, under 510(k) number K880615.

Who is the listed applicant for AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30?

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

What is the FDA product code for AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30?

The FDA product code for AMBULATORY ECG DIGITAL MONITOR MODEL: TD-30 is DXH. This falls under the Hematology category.

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: DXH)

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.

K250233PreemptiveAI Clinical SDKMeasure Labs, Inc. (Dba Preemptiveai, Inc.)K250258HeartBeam AIMIGo with 12-L ECG Synthesis Software SystemHeartbeam, Inc.K243438MEMO Patch M (MPT-E08R-UNC01)Huinno Co., Ltd.K243981Hexoskin Medical System (7100-00016)Carre Technologies, Inc.K243003VitalSigns 1-Lead Holter (VSH101)VitalSigns Technology Co., Ltd.K233521QT ECG (QTERD100)QT Medical, 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.

↑