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FDA 510(k)

VARIAN NASOPHARYNX APPLICATOR

K-Number: K042360 · 2005-02-16

ApplicantVarian Medical Systems, Inc.
Decision Date2005-02-16
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIAN NASOPHARYNX APPLICATOR 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 2005-02-16 under 510(k) number K042360. 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 NASOPHARYNX APPLICATOR?

VARIAN NASOPHARYNX APPLICATOR is a medical device that received FDA 510(k) clearance on 2005-02-16. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K042360.

When did VARIAN NASOPHARYNX APPLICATOR receive FDA 510(k) clearance?

VARIAN NASOPHARYNX APPLICATOR received FDA 510(k) clearance on 2005-02-16, under 510(k) number K042360.

Who is the listed applicant for VARIAN NASOPHARYNX APPLICATOR?

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 NASOPHARYNX APPLICATOR?

The FDA product code for VARIAN NASOPHARYNX APPLICATOR is JAQ.

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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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