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FDA 510(k)

CARDIOVATIONS RETRACTOR

K-Number: K031847 · 2003-07-21

ApplicantETHICON, Inc.
Decision Date2003-07-21
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CARDIOVATIONS RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2003-07-21 under 510(k) number K031847. 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 RETRACTOR?

CARDIOVATIONS RETRACTOR is a medical device that received FDA 510(k) clearance on 2003-07-21. The listed applicant is ETHICON, Inc.. The 510(k) number is K031847.

When did CARDIOVATIONS RETRACTOR receive FDA 510(k) clearance?

CARDIOVATIONS RETRACTOR received FDA 510(k) clearance on 2003-07-21, under 510(k) number K031847.

Who is the listed applicant for CARDIOVATIONS RETRACTOR?

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 RETRACTOR?

The FDA product code for CARDIOVATIONS RETRACTOR 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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