Victoreen, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
40
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K982937MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBERNovember 19, 1998
K974112VACUDAP, MODEL 2000, 2001January 29, 1998
K973960MODEL 37-185January 14, 1998
K964952VERIDOSE V (FIVE), MODEL NUMBER 37-705July 21, 1997
K964785VERIDOSE DIODESJune 13, 1997
K971382PRONE BREAST POSITIONING BOARD, MODEL #37-018June 6, 1997
K952233CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628June 16, 1995
K940660MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEMDecember 9, 1994
K935435NUCLEAR ASSOC 37-08 SER, RAYCAST HP RADIO IMMOB SYSTJuly 29, 1994
K941931DIAGNOSTIC X-RAY PATIENT EXPOSURE INDICATORMay 26, 1994
K934549ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELDFebruary 19, 1994
K935397NUCLEAR ASSOCIATES KNIGHT SR., KNIGHT JR. AND SESAM PORTABLE RADIOGRAPHY CASSETTE HOLDERSDecember 15, 1993
K932342MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBERDecember 13, 1993
K934850NUCLEAR ASSOCIATES PERSONNEL PROTECTIVE SHIELDSNovember 22, 1993
K931927VICTOREEN MODEL 530November 15, 1993
K934548ALL-VUE & GAMMA-VUE VIAL SHIELDSNovember 12, 1993
K934362NUCLEAR ASSOCIATES GLASSERSNovember 12, 1993
K931657NUCLEAR ASSOCIATES MODEL 34-070 BRACHYTHERAPY CAL.July 27, 1993
K911340AUTOCOMPAugust 26, 1991
K90093237-702 AND 37-703 PC RAINBOWDecember 5, 1990