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FDA 510(k)

CENTERING INTRALUMINAL APPLICATOR

K-Number: K082653 · 2008-10-10

ApplicantVarian Medical Systems, Inc.
Decision Date2008-10-10
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CENTERING INTRALUMINAL 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 2008-10-10 under 510(k) number K082653. 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 CENTERING INTRALUMINAL APPLICATOR?

CENTERING INTRALUMINAL APPLICATOR is a medical device that received FDA 510(k) clearance on 2008-10-10. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K082653.

When did CENTERING INTRALUMINAL APPLICATOR receive FDA 510(k) clearance?

CENTERING INTRALUMINAL APPLICATOR received FDA 510(k) clearance on 2008-10-10, under 510(k) number K082653.

Who is the listed applicant for CENTERING INTRALUMINAL 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 CENTERING INTRALUMINAL APPLICATOR?

The FDA product code for CENTERING INTRALUMINAL 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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