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510(k) K932342

MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBER by Victoreen, Inc. — Product Code LNN

K932342 is an FDA 510(k) premarket notification submitted by Victoreen, Inc. for the device "MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBER". The FDA issued a decision of Substantially Equivalent on December 13, 1993. Victoreen, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 13, 1993
Date Received
May 14, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Victoreen, Inc.

  • K982937 — MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBER (November 19, 1998)
  • K974112 — VACUDAP, MODEL 2000, 2001 (January 29, 1998)
  • K973960 — MODEL 37-185 (January 14, 1998)
  • K964952 — VERIDOSE V (FIVE), MODEL NUMBER 37-705 (July 21, 1997)
  • K964785 — VERIDOSE DIODES (June 13, 1997)
  • K971382 — PRONE BREAST POSITIONING BOARD, MODEL #37-018 (June 6, 1997)
  • K952233 — CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628 (June 16, 1995)
  • K940660 — MODEL 37-720 DUAL DIODE DOSIMETRY SYSTEM (December 9, 1994)
  • K935435 — NUCLEAR ASSOC 37-08 SER, RAYCAST HP RADIO IMMOB SYST (July 29, 1994)
  • K941931 — DIAGNOSTIC X-RAY PATIENT EXPOSURE INDICATOR (May 26, 1994)

Other clearances for product code LNN

  • K901881 — VIBROMETRY SYSTEM (May 31, 1991)

FDA data resources