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FDA 510(k)

Varian Cervical Sleeves

K-Number: K172675 · 2018-05-16

ApplicantVarian Medical Systems, Inc.
Decision Date2018-05-16
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Varian Cervical Sleeves 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 2018-05-16 under 510(k) number K172675. 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 Cervical Sleeves?

Varian Cervical Sleeves is a medical device that received FDA 510(k) clearance on 2018-05-16. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K172675.

When did Varian Cervical Sleeves receive FDA 510(k) clearance?

Varian Cervical Sleeves received FDA 510(k) clearance on 2018-05-16, under 510(k) number K172675.

Who is the listed applicant for Varian Cervical Sleeves?

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 Cervical Sleeves?

The FDA product code for Varian Cervical Sleeves is JAQ.

Other records listing Varian Medical Systems, Inc. as applicant

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Related Devices (Code: JAQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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