FDA 510(k) Applications Submitted by GLEN IMPAL

FDA 510(k) Number Submission Date Device Name Applicant
K960839 02/26/1996 FILM SCANNER 300 CANNON U.S.A., INC.
K980246 01/23/1998 NON-MYDRIATIC RETINAL CAMERA, MODEL CR6-45NM CANON U.S.A., INC.
K981556 05/01/1998 CANON X-RAY DIGITAL CAMERA CXDI-11 CANON U.S.A., INC.
K963079 08/07/1996 CANON TX-10 TONOMETER CANON U.S.A., INC.


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