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510(k) K022154

LEVEL 356 X-RAY FILM PROCESSOR, MODELS MD & MD-D by Fischer Industries, Inc. — Product Code IXW

K022154 is an FDA 510(k) premarket notification submitted by Fischer Industries, Inc. for the device "LEVEL 356 X-RAY FILM PROCESSOR, MODELS MD & MD-D". The FDA issued a decision of Substantially Equivalent on September 30, 2002. The device falls under product code IXW (Processor, Radiographic-Film, Automatic), a Class II device regulated under 21 CFR 892.1900. Fischer Industries, Inc. has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 30, 2002
Date Received
July 2, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Processor, Radiographic-Film, Automatic
Device Class
Class II
Regulation Number
892.1900
Review Panel
RA
Submission Type

Other clearances by Fischer Industries, Inc.

  • K940112 — X-RAY FILM PROCESSOR (April 11, 1995)
  • K861837 — FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND (August 7, 1986)

Other clearances for product code IXW

  • K111167 — XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINT (August 18, 2011)
  • K093503 — INTRAX FILM PROCESSOR (January 6, 2010)
  • K091628 — OPTIMAX, COMPACT 2, OPTIMAX 2010, ECOMAX (August 21, 2009)
  • K024342 — RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000 (April 23, 2003)
  • K023825 — FILM PROCESSOR, MODEL LIFE RAY PRO 2500 (February 12, 2003)
  • K023801 — FILM PROCESSOR, MODEL LIFE RAY PRO 1000 (February 12, 2003)
  • K023613 — AX200 AUTOMATIC X-RAY FILM PROCESSOR, MODEL 6586.036 (January 23, 2003)
  • K002640 — FREEDOM AUTOMATIC FILM PROCESSOR (November 8, 2000)
  • K002404 — MICRO-MAX, MODEL 319 (August 30, 2000)
  • K001321 — ALL-PRO 2010 (May 16, 2000)

FDA data resources