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)

IMS-2000R RESTING ELECTROCARDIOGRAPHIC SYSTEM

K-Number: K870934 · 1987-05-06

Decision Date1987-05-06
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IMS-2000R RESTING ELECTROCARDIOGRAPHIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Integrated Medical Systems, Inc.. It received FDA 510(k) clearance on 1987-05-06 under 510(k) number K870934. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMS-2000R RESTING ELECTROCARDIOGRAPHIC SYSTEM?

IMS-2000R RESTING ELECTROCARDIOGRAPHIC SYSTEM is a medical device that received FDA 510(k) clearance on 1987-05-06. The listed applicant is Integrated Medical Systems, Inc.. The 510(k) number is K870934.

When did IMS-2000R RESTING ELECTROCARDIOGRAPHIC SYSTEM receive FDA 510(k) clearance?

IMS-2000R RESTING ELECTROCARDIOGRAPHIC SYSTEM received FDA 510(k) clearance on 1987-05-06, under 510(k) number K870934.

Who is the listed applicant for IMS-2000R RESTING ELECTROCARDIOGRAPHIC SYSTEM?

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

What is the FDA product code for IMS-2000R RESTING ELECTROCARDIOGRAPHIC SYSTEM?

The FDA product code for IMS-2000R RESTING ELECTROCARDIOGRAPHIC SYSTEM is DXG.

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 Integrated Medical Systems, 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: DXG)

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.

↑