510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850838Substantially Equivalent

Clinicomp Rdms Radionuclide Dispensing Mgmt. Softw

Clinicomp, Inc., Huntington Woods MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850838 is the FDA 510(k) clearance record for CLINICOMP RDMS RADIONUCLIDE DISPENSING MGMT. SOFTW, a class II device, cleared for Clinicomp, Inc. on under FDA product code KPT (Calibrator, Dose, Radionuclide). FDA records list 3 510(k) clearances for Clinicomp, Inc., from to . As of , FDA records show no recalls naming K850838.

Clearance record

Decision date
Received
(209 days to decision)
Product code
KPT Calibrator, Dose, Radionuclide
Regulation
21 CFR 892.1360
Device class
Class II
Review panel
Radiology
Applicant
Clinicomp, Inc. P.O. Box 7070, Huntington Woods MI
Third party review
No

Clearances, product code KPT

Trailing 12 months

FDA records hold no clearances under product code KPT in the trailing twelve months.

FDA records show no clearances under product code KPT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KPT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260