FDA 510(k)

VPC

K-Number: K190345 · 2019-05-16

Decision Date2019-05-16

Product CodeCAZ

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

VPC is a medical device manufactured by PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2019-05-16 under approval number K190345. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VPC?

VPC is a medical device that received FDA 510(k) clearance on 2019-05-16. It is manufactured by PAJUNK GmbH Medizintechnologie. The 510(k) number is K190345.

When was VPC approved by the FDA?

VPC received FDA 510(k) clearance on 2019-05-16, under approval number K190345.

What company makes VPC?

VPC is manufactured by PAJUNK GmbH Medizintechnologie.

What is the FDA product code for VPC?

The FDA product code for VPC is CAZ.

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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.