Medical Device Manufacturer · US , Mchenry , IL

Victoreen, Inc. - FDA 510(k) Cleared Devices

40 submissions · 40 cleared · Since 1979

Total

Cleared

Denied

Victoreen, Inc. has 40 FDA 510(k) cleared radiology devices. Based in Mchenry, US.

Historical record: 40 cleared submissions from 1979 to 1998.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Victoreen, Inc.

40 devices

1-12 of 40

Cleared Nov 19, 1998

MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBER

K982937 · LHN

Radiology · 90d

Cleared Jan 29, 1998

VACUDAP, MODEL 2000, 2001

VERIDOSE V (FIVE), MODEL NUMBER 37-705

PRONE BREAST POSITIONING BOARD, MODEL #37-018

K971382 · IYE

Radiology · 84d

Cleared Jun 16, 1995

CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628

K952233 · EAK

Radiology · 35d

Cleared Dec 09, 1994

MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM

K940660 · IYE

Radiology · 297d

Cleared Jul 29, 1994

NUCLEAR ASSOC 37-08 SER, RAYCAST HP RADIO IMMOB SYST

K935435 · IYE

Radiology · 261d

Cleared May 26, 1994

DIAGNOSTIC X-RAY PATIENT EXPOSURE INDICATOR

K941931 · KPR

Radiology · 36d

Cleared Feb 19, 1994

ALL-VUE ULTRA-LITE THIN WALL SYRINGE SHIELD

K934549 · IWR

Radiology · 150d

Cleared Dec 15, 1993

NUCLEAR ASSOCIATES KNIGHT SR., KNIGHT JR. AND SESAM PORTABLE RADIOGRAPHY...

K935397 · IXA

Radiology · 36d

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Victoreen, Inc. - FDA 510(k) Cleared Devices

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