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FDA 510(k)

CARDIOVATIONS PORTABLE VIDEO SYSTEM

K-Number: K032339 · 2003-08-08

ApplicantETHICON, Inc.
Decision Date2003-08-08
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CARDIOVATIONS PORTABLE VIDEO SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2003-08-08 under 510(k) number K032339. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOVATIONS PORTABLE VIDEO SYSTEM?

CARDIOVATIONS PORTABLE VIDEO SYSTEM is a medical device that received FDA 510(k) clearance on 2003-08-08. The listed applicant is ETHICON, Inc.. The 510(k) number is K032339.

When did CARDIOVATIONS PORTABLE VIDEO SYSTEM receive FDA 510(k) clearance?

CARDIOVATIONS PORTABLE VIDEO SYSTEM received FDA 510(k) clearance on 2003-08-08, under 510(k) number K032339.

Who is the listed applicant for CARDIOVATIONS PORTABLE VIDEO SYSTEM?

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

What is the FDA product code for CARDIOVATIONS PORTABLE VIDEO SYSTEM?

The FDA product code for CARDIOVATIONS PORTABLE VIDEO SYSTEM is GCJ.

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Related Devices (Code: GCJ)

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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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