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FDA 510(k)

Varian Sterilization Boxes

K-Number: K160021 · 2016-04-13

ApplicantVarian Medical Systems, Inc.
Decision Date2016-04-13
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Varian Sterilization Boxes is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2016-04-13 under approval number K160021. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Varian Sterilization Boxes?

Varian Sterilization Boxes is a medical device that received FDA 510(k) clearance on 2016-04-13. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K160021.

When was Varian Sterilization Boxes approved by the FDA?

Varian Sterilization Boxes received FDA 510(k) clearance on 2016-04-13, under approval number K160021.

What company makes Varian Sterilization Boxes?

Varian Sterilization Boxes is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for Varian Sterilization Boxes?

The FDA product code for Varian Sterilization Boxes is JAQ.

Other Devices by Varian Medical Systems, Inc.

K162476Varian High Energy Linear Accelerator K160045Heyman Packing Applicator Set K161540Advanced Breast Template System K161576Esophagus Bougie Set K160516Universal Cylinder Applicator Family, Universal Segmented Cylinder Applicator Set, Universal Stump Applicator Set, Universal Cervix Probe Set, odd lengths, Universal Cervix Probe Set, even lengths K162533Kelowna GYN and Crook Prostate Templates

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Related Devices (Code: JAQ)

K160045Heyman Packing Applicator SetVarian Medical Systems, Inc. K161540Advanced Breast Template SystemVarian Medical Systems, Inc. K161576Esophagus Bougie SetVarian Medical Systems, Inc. K160516Universal Cylinder Applicator Family, Universal Segmented Cylinder Applicator Set, Universal Stump Applicator Set, Universal Cervix Probe Set, odd lengths, Universal Cervix Probe Set, even lengthsVarian Medical Systems, Inc. K150979CT/MR Compatible M.A.C. Interstitial GYN TemplateMick Radio-Nuclear Instruments, Inc. K162533Kelowna GYN and Crook Prostate TemplatesVarian Medical Systems, 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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