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FDA 510(k)

VITALCOR FEATHERWEIGHT VASCULAR CLAMPS

K-Number: K070661 · 2007-08-29

ApplicantVitalcor, Inc.
Decision Date2007-08-29
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITALCOR FEATHERWEIGHT VASCULAR CLAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Vitalcor, Inc.. It received FDA 510(k) clearance on 2007-08-29 under 510(k) number K070661. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALCOR FEATHERWEIGHT VASCULAR CLAMPS?

VITALCOR FEATHERWEIGHT VASCULAR CLAMPS is a medical device that received FDA 510(k) clearance on 2007-08-29. The listed applicant is Vitalcor, Inc.. The 510(k) number is K070661.

When did VITALCOR FEATHERWEIGHT VASCULAR CLAMPS receive FDA 510(k) clearance?

VITALCOR FEATHERWEIGHT VASCULAR CLAMPS received FDA 510(k) clearance on 2007-08-29, under 510(k) number K070661.

Who is the listed applicant for VITALCOR FEATHERWEIGHT VASCULAR CLAMPS?

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

What is the FDA product code for VITALCOR FEATHERWEIGHT VASCULAR CLAMPS?

The FDA product code for VITALCOR FEATHERWEIGHT VASCULAR CLAMPS is DXC.

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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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