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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 the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2016-04-13 under 510(k) 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. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K160021.

When did Varian Sterilization Boxes receive FDA 510(k) clearance?

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

Who is the listed applicant for Varian Sterilization Boxes?

The FDA 510(k) record lists Varian Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Varian Sterilization Boxes?

The FDA product code for Varian Sterilization Boxes is JAQ.

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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.

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