Victoreen, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBER, VACUDAP, MODEL 2000, 2001, MODEL 37-185
40
Total
40
Cleared
0
Denied
FDA 510(k) Regulatory Record - Victoreen, Inc. Radiology ✕
40 devices
Cleared
Nov 19, 1998
MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBER
Radiology
90d
Cleared
Jan 29, 1998
VACUDAP, MODEL 2000, 2001
Radiology
90d
Cleared
Jan 14, 1998
MODEL 37-185
Radiology
90d
Cleared
Jul 21, 1997
VERIDOSE V (FIVE), MODEL NUMBER 37-705
Radiology
223d
Cleared
Jun 13, 1997
VERIDOSE DIODES
Radiology
196d
Cleared
Jun 06, 1997
PRONE BREAST POSITIONING BOARD, MODEL #37-018
Radiology
84d
Cleared
Jun 16, 1995
CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628
Radiology
35d
Cleared
Dec 09, 1994
MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM
Radiology
297d
Cleared
Jul 29, 1994
NUCLEAR ASSOC 37-08 SER, RAYCAST HP RADIO IMMOB SYST
Radiology
261d
Cleared
May 26, 1994
DIAGNOSTIC X-RAY PATIENT EXPOSURE INDICATOR
Radiology
36d
Cleared
Feb 19, 1994
ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD
Radiology
150d
Cleared
Dec 15, 1993
NUCLEAR ASSOCIATES KNIGHT SR., KNIGHT JR. AND SESAM PORTABLE RADIOGRAPHY...
Radiology
36d
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