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FDA 510(k) Applications Submitted by HILLARD WELCH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030054
01/06/2003
DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSES
FCI OPHTHALMICS, INC.
K110554
02/28/2011
BIOCERAMIC ORBITAL IMPLANT, ORBTEX
CERAMISYS LTD.
K980840
03/04/1998
LOKKI DT
HILLARD W. WELCH
K001125
04/07/2000
GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING
GEUDER GMBH
K961658
04/29/1996
MEGATRON OPHTHALMIC SURGICAL SYSTEM
INTL. OPHTHALMIC INDUSTRIES CORP.
K061398
05/19/2006
SNUG PLUG PUNCTUM PLUG
FCI OPHTHALMICS, INC.
K061404
05/19/2006
MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
FCI OPHTHALMICS, INC.
K023400
10/09/2002
FCI MESH WRAPPED BIOCERAMIC ORBITAL IMPLANT
FCI OPHTHALMICS, INC.
K023758
11/08/2002
BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)
FCI OPHTHALMICS, INC.
K994028
11/26/1999
FLIPO XENON CURING LIGHT
LOKKI
K974603
12/10/1997
PLAQUAGRAFE, AGRAFE P4V
ATLAS TECHNOLOGY
K103820
12/30/2010
REPROBONE DENTAL GRAFTING MATERIAL
CERAMISYS LTD
K024374
12/31/2002
RMO PLASMA CURING LIGHT
LOKKI LASERS MEDICAUX
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