FDA 510(k)

CC-100

K-Number: K811016 · 1981-05-01

Decision Date1981-05-01

Product CodeDPS

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CC-100 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 1981-05-01 under 510(k) number K811016. 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 CC-100?

CC-100 is a medical device that received FDA 510(k) clearance on 1981-05-01. The listed applicant is Anthro-Metrics Corp.. The 510(k) number is K811016.

When did CC-100 receive FDA 510(k) clearance?

CC-100 received FDA 510(k) clearance on 1981-05-01, under 510(k) number K811016.

Who is the listed applicant for CC-100?

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-100?

The FDA product code for CC-100 is DPS.

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 SYSTEMS K811527CC-103 K802312CC101 ECG MONITORING SYSTEM

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.