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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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