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FDA 510(k)

INTERSTITIAL NEEDLES

K-Number: K073133 · 2007-11-16

ApplicantVarian Medical Systems, Inc.
Decision Date2007-11-16
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTERSTITIAL 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 2007-11-16 under 510(k) number K073133. 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 INTERSTITIAL NEEDLES?

INTERSTITIAL NEEDLES is a medical device that received FDA 510(k) clearance on 2007-11-16. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K073133.

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

INTERSTITIAL NEEDLES received FDA 510(k) clearance on 2007-11-16, under 510(k) number K073133.

Who is the listed applicant for INTERSTITIAL 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 INTERSTITIAL NEEDLES?

The FDA product code for INTERSTITIAL 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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