Home / 510(k) Clearances / K843148

510(k) K843148

KODAK T-MAT H FILM SO-118 by Eastman Kodak Company — Product Code LWZ

K843148 is an FDA 510(k) premarket notification submitted by Eastman Kodak Company for the device "KODAK T-MAT H FILM SO-118". The FDA issued a decision of Substantially Equivalent on August 27, 1984. The device falls under product code LWZ (Tissue Graft Of Less Than 6mm), a Class III device. Eastman Kodak Company has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 27, 1984
Date Received
August 10, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tissue Graft Of Less Than 6mm
Device Class
Class III
Regulation Number
Review Panel
CV
Submission Type

Other clearances by Eastman Kodak Company

  • K060550 — KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386 (March 31, 2006)
  • K060137 — KODAK ECLIPSE IMAGE PROCESSING SOFTWARE (March 16, 2006)
  • K060079 — KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM (February 8, 2006)
  • K060055 — KODAK PACS (February 7, 2006)
  • K053347 — KODAK CARESTREAM PACS (January 4, 2006)
  • K051483 — KODAK DIRECTVIEW DR SYSTEM DETECTOR (June 21, 2005)
  • K051258 — KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345 (June 1, 2005)
  • K042159 — KODAK COLOR MEDICAL IMAGER 1000 (September 24, 2004)
  • K042158 — KODAK MEDICAL IMAGER 300 (September 24, 2004)
  • K040378 — KODAK DIRECTVIEW CR CASSETTE/GP/15 X 30 CM, CATALOG# 8418253 (May 24, 2004)

Other clearances for product code LWZ

  • K843149 — KODAK T-MAT C FILM SO-119 (August 27, 1984)

FDA data resources