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FDA 510(k)

Heyman Packing Applicator Set

K-Number: K160045 · 2016-11-17

ApplicantVarian Medical Systems, Inc.
Decision Date2016-11-17
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Heyman Packing Applicator Set 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 2016-11-17 under 510(k) number K160045. 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 Heyman Packing Applicator Set?

Heyman Packing Applicator Set is a medical device that received FDA 510(k) clearance on 2016-11-17. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K160045.

When did Heyman Packing Applicator Set receive FDA 510(k) clearance?

Heyman Packing Applicator Set received FDA 510(k) clearance on 2016-11-17, under 510(k) number K160045.

Who is the listed applicant for Heyman Packing Applicator Set?

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 Heyman Packing Applicator Set?

The FDA product code for Heyman Packing Applicator Set 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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