FDA 510(k) Applications Submitted by DUTCH OPHTHALMIC USA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K010082 01/10/2001 D.O.R.C. HARMONY TOTAL TTC VITRECTOMY SYSTEM DUTCH OPHTHALMIC USA, INC.
K980636 02/19/1998 FIBER OPTIC ENDOILLUMINATION PROBE DUTCH OPHTHALMIC USA, INC.
K962135 06/03/1996 D.O.R.C. MICRODIATHERMY SYSTEM DUTCH OPHTHALMIC USA, INC.
K012821 08/23/2001 D.O.R.C. CRYOSTAR CRYOSURGICAL SYSTEM DUTCH OPHTHALMIC USA, INC.
K973229 08/27/1997 D.O.R.C. HEXON ILLUMINATION SYSTEM DUTCH OPHTHALMIC USA, INC.
K973757 10/02/1997 D.O.R.C. SOLUX LIGHT SOURCE DUTCH OPHTHALMIC USA, INC.
K954842 10/23/1995 D.O.R.C. VFI/VFE SYSTEM DUTCH OPHTHALMIC USA, INC.
K983797 10/28/1998 D.O.R.C. HARMONY TOTAL VITRECTOMY SYSTEM DUTCH OPHTHALMIC USA, INC.


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