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FDA 510(k)

Aesculap Video Assisted Thoracic Surgery (VATS) INstruments

K-Number: K170683 · 2018-02-20

Decision Date2018-02-20
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Aesculap Video Assisted Thoracic Surgery (VATS) INstruments is a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2018-02-20 under approval number K170683. 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 Aesculap Video Assisted Thoracic Surgery (VATS) INstruments?

Aesculap Video Assisted Thoracic Surgery (VATS) INstruments is a medical device that received FDA 510(k) clearance on 2018-02-20. It is manufactured by Aesculap, Inc.. The 510(k) number is K170683.

When was Aesculap Video Assisted Thoracic Surgery (VATS) INstruments approved by the FDA?

Aesculap Video Assisted Thoracic Surgery (VATS) INstruments received FDA 510(k) clearance on 2018-02-20, under approval number K170683.

What company makes Aesculap Video Assisted Thoracic Surgery (VATS) INstruments?

Aesculap Video Assisted Thoracic Surgery (VATS) INstruments is manufactured by Aesculap, Inc..

What is the FDA product code for Aesculap Video Assisted Thoracic Surgery (VATS) INstruments?

The FDA product code for Aesculap Video Assisted Thoracic Surgery (VATS) INstruments is GCJ.

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Official Source

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