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FDA 510(k)

STERIZONE(R) VP4 Sterilizer

K-Number: K190260 · 2019-07-19

ApplicantTso3, Inc.
Decision Date2019-07-19
Product CodePJJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERIZONE(R) VP4 Sterilizer is a medical device manufactured by Tso3, Inc.. It received FDA 510(k) clearance on 2019-07-19 under approval number K190260. The device is classified under product code PJJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERIZONE(R) VP4 Sterilizer?

STERIZONE(R) VP4 Sterilizer is a medical device that received FDA 510(k) clearance on 2019-07-19. It is manufactured by Tso3, Inc.. The 510(k) number is K190260.

When was STERIZONE(R) VP4 Sterilizer approved by the FDA?

STERIZONE(R) VP4 Sterilizer received FDA 510(k) clearance on 2019-07-19, under approval number K190260.

What company makes STERIZONE(R) VP4 Sterilizer?

STERIZONE(R) VP4 Sterilizer is manufactured by Tso3, Inc..

What is the FDA product code for STERIZONE(R) VP4 Sterilizer?

The FDA product code for STERIZONE(R) VP4 Sterilizer is PJJ.

Other Devices by Tso3, Inc.

K153689STERIZONE Sterilizer K172191STERIZONE VP4 Sterilizer K173694STERIZONE VP4 Sterilizer

Related Devices (Code: PJJ)

K153689STERIZONE SterilizerTso3, Inc. K153392STERIZONE VP4 SterilizerTs03, Inc. K172191STERIZONE VP4 SterilizerTso3, Inc. K173694STERIZONE VP4 SterilizerTso3, Inc.

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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