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FDA 510(k)

VALENCIA SKIN APPLICATOR SET, MODEL: 189.701

K-Number: K073107 · 2007-12-07

ApplicantNucletron Corporation
Decision Date2007-12-07
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VALENCIA SKIN APPLICATOR SET, MODEL: 189.701 is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron Corporation. It received FDA 510(k) clearance on 2007-12-07 under 510(k) number K073107. 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 VALENCIA SKIN APPLICATOR SET, MODEL: 189.701?

VALENCIA SKIN APPLICATOR SET, MODEL: 189.701 is a medical device that received FDA 510(k) clearance on 2007-12-07. The listed applicant is Nucletron Corporation. The 510(k) number is K073107.

When did VALENCIA SKIN APPLICATOR SET, MODEL: 189.701 receive FDA 510(k) clearance?

VALENCIA SKIN APPLICATOR SET, MODEL: 189.701 received FDA 510(k) clearance on 2007-12-07, under 510(k) number K073107.

Who is the listed applicant for VALENCIA SKIN APPLICATOR SET, MODEL: 189.701?

The FDA 510(k) record lists Nucletron Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VALENCIA SKIN APPLICATOR SET, MODEL: 189.701?

The FDA product code for VALENCIA SKIN APPLICATOR SET, MODEL: 189.701 is JAQ.

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Other records listing Nucletron Corporation as applicant

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Related Devices (Code: JAQ)

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K262383LumenCare AzureNucletron B.V.K252717MAASTRO Rectal Applicator SetVarian Medical SystemsK251037Rectal ApplicatorNucletron B.V.K252884Guided Aarhus Applicator SetVarian Medical SystemsK250299CT/ MR Tandem and Ovoid SetVarian Medical Systems, Inc.K250289Intracavitary/Interstitial SystemVarian Medical Systems

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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