UTRECHT INTERSTITIAL FLETCHER CT/MR APPLICATOR SET, MODEL 110.270, INTERSTITIAL RING CT/MR APPLICATOR SET,MODEL 110.330,— 510(k) K091154

Name: FDA 510(k) clearance K091154
Creator: U.S. Food and Drug Administration
Published: 2009-05-18

Substantially Equivalent

Nucletron Corporation

FDA 510(k) clearance K091154 for UTRECHT INTERSTITIAL FLETCHER CT/MR APPLICATOR SET, MODEL 110.270, INTERSTITIAL RING CT/MR APPLICATOR SET,MODEL 110.330,, Substantially Equivalent on 2009-05-18. Applicant: Nucletron Corporation. Device class: 2.

Clearance details

Applicant: Nucletron Corporation
Product code: Code JAQ
Device class: Class 2
Regulation: 21 CFR 892.5700
Advisory panel: Radiology
Date received: 2009-04-21
Decision date: 2009-05-18
Decision: Substantially Equivalent
Clearance type: Special
Location: Columbia, MD, US

Download summary PDF View on FDA.gov ↗

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