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FDA 510(k)

VARIAN INTERSTITIAL TITANIUM NEEDLES

K-Number: K093291 · 2009-11-17

ApplicantVarian Medical Systems, Inc.
Decision Date2009-11-17
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIAN INTERSTITIAL TITANIUM NEEDLES 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 2009-11-17 under 510(k) number K093291. 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 INTERSTITIAL TITANIUM NEEDLES?

VARIAN INTERSTITIAL TITANIUM NEEDLES is a medical device that received FDA 510(k) clearance on 2009-11-17. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K093291.

When did VARIAN INTERSTITIAL TITANIUM NEEDLES receive FDA 510(k) clearance?

VARIAN INTERSTITIAL TITANIUM NEEDLES received FDA 510(k) clearance on 2009-11-17, under 510(k) number K093291.

Who is the listed applicant for VARIAN INTERSTITIAL TITANIUM NEEDLES?

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 INTERSTITIAL TITANIUM NEEDLES?

The FDA product code for VARIAN INTERSTITIAL TITANIUM NEEDLES is JAQ.

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Related Devices (Code: 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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