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FDA 510(k)

VFS1 Bipolar Electrosurgical Generator

K-Number: K200169 · 2020-05-14

ApplicantFHC, Inc.
Decision Date2020-05-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VFS1 Bipolar Electrosurgical Generator is a medical device manufactured by FHC, Inc.. It received FDA 510(k) clearance on 2020-05-14 under approval number K200169. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VFS1 Bipolar Electrosurgical Generator?

VFS1 Bipolar Electrosurgical Generator is a medical device that received FDA 510(k) clearance on 2020-05-14. It is manufactured by FHC, Inc.. The 510(k) number is K200169.

When was VFS1 Bipolar Electrosurgical Generator approved by the FDA?

VFS1 Bipolar Electrosurgical Generator received FDA 510(k) clearance on 2020-05-14, under approval number K200169.

What company makes VFS1 Bipolar Electrosurgical Generator?

VFS1 Bipolar Electrosurgical Generator is manufactured by FHC, Inc..

What is the FDA product code for VFS1 Bipolar Electrosurgical Generator?

The FDA product code for VFS1 Bipolar Electrosurgical Generator is GEI.

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Official Source

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