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FDA 510(k)

PC-180 / PRINCE 180 EASY ECG MONITOR

K-Number: K073152 · 2008-01-10

ApplicantShenzhen Creative Industry Co., Ltd.
Decision Date2008-01-10
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PC-180 / PRINCE 180 EASY ECG MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Creative Industry Co., Ltd.. It received FDA 510(k) clearance on 2008-01-10 under 510(k) number K073152. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PC-180 / PRINCE 180 EASY ECG MONITOR?

PC-180 / PRINCE 180 EASY ECG MONITOR is a medical device that received FDA 510(k) clearance on 2008-01-10. The listed applicant is Shenzhen Creative Industry Co., Ltd.. The 510(k) number is K073152.

When did PC-180 / PRINCE 180 EASY ECG MONITOR receive FDA 510(k) clearance?

PC-180 / PRINCE 180 EASY ECG MONITOR received FDA 510(k) clearance on 2008-01-10, under 510(k) number K073152.

Who is the listed applicant for PC-180 / PRINCE 180 EASY ECG MONITOR?

The FDA 510(k) record lists Shenzhen Creative Industry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PC-180 / PRINCE 180 EASY ECG MONITOR?

The FDA product code for PC-180 / PRINCE 180 EASY ECG MONITOR is DSH.

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Related Devices (Code: DSH)

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.

K260157LifeLens Physiological MonitorLifeLens Technologies, Inc.K252389Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)Smwmed, Inc.K253293VitaloJAK Clinic (Model 7100)Vitalograph , Ltd.K243650Zio® monitor (DFG0001)iRhythm Technologies, Inc.K243603AeviceMDAevice Health Pte. , Ltd.K242583AT-Patch (ATP-C130/ATP-C70)Atsens Co., Ltd.

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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