510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K081281Substantially Equivalent

Ocentra Masterplan 3.1 (Ocentra Brachy)

Nucletron BV, Columbia MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K081281 is the FDA 510(k) clearance record for OCENTRA MASTERPLAN 3.1 (OCENTRA BRACHY), a class II device, cleared for Nucletron Corporation on under FDA product code MUJ (System, Planning, Radiation Therapy Treatment). FDA records list 61 510(k) clearances for Nucletron Corporation, from to . As of , FDA records show 2 recalls naming K081281.

Clearance record

Decision date
Received
(14 days to decision)
Product code
MUJ System, Planning, Radiation Therapy Treatment
Regulation
21 CFR 892.5050
Device class
Class II
Review panel
Radiology
Applicant
Nucletron Corporation 8671 Robert Fulton Dr., Columbia MD
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code MUJ

Trailing 12 months
12 clearances under product code MUJ in the twelve months to October 2026, December 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code MUJ, trailing twelve months
MonthClearances
November 20251
December 20253
January 20260
February 20262
March 20261
April 20260
May 20263
June 20261
July 20261
August 20260
September 20260
October 20260