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FDA 510(k)

CC-103

K-Number: K811527 · 1981-06-16

ApplicantAnthro-Metrics Corp.
Decision Date1981-06-16
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CC-103 is the device name listed in this FDA 510(k) record. The listed applicant is Anthro-Metrics Corp.. It received FDA 510(k) clearance on 1981-06-16 under 510(k) number K811527. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CC-103?

CC-103 is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is Anthro-Metrics Corp.. The 510(k) number is K811527.

When did CC-103 receive FDA 510(k) clearance?

CC-103 received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811527.

Who is the listed applicant for CC-103?

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

What is the FDA product code for CC-103?

The FDA product code for CC-103 is DSI.

Other records listing Anthro-Metrics Corp. 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.

K813287CC-201 ECG MONITORING SYSTEMSK811016CC-100K802312CC101 ECG MONITORING SYSTEM

Related Devices (Code: DSI)

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.

K243349BodyGuardian Remote Monitoring System (BGRMS v3.0)Boston Scientific Cardiac Diagnostic Technologies, Inc.K250356MoMe ARC® Wireless Ambulatory ECG Monitoring and Detection System (32000)Infobionic, Inc.K240177Zio AT® device (A100A1001)iRhythm Technologies, Inc.K230265MoMe® ARC Wireless Ambulatory ECG Monitoring and Detection SystemInfobionic, Inc.K231276SmartCardia 7L PlatformSmartcardia SAK193104Unified Arrhythmia Diagnostic System PocketECG IVMedicalgorithmics S.A.

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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