FDA 510(k) Applications Submitted by ANNE BOHSACK
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K980816 |
03/03/1998 |
RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES |
FCI OPHTHALMICS, INC. |
K980822 |
03/03/1998 |
TITANIUM PEG SYSTEM |
FCI OPHTHALMICS, INC. |
K991238 |
04/12/1999 |
FCI CRAWFORD PROBE INTUBATION SETS |
FCI OPHTHALMICS, INC. |
K961909 |
05/16/1996 |
READY-SET PUNCTAL PLUGS |
FCI OPHTHALMICS, INC. |
K992294 |
07/07/1999 |
BIOCERAMIC ORBITAL IMPLANT |
FCI OPHTHALMICS, INC. |
K963219 |
08/16/1996 |
RETINAL DETACHMENT IMPLANTS; INCLUDING BANS, STRIPS, TIRES, SLEEVES, CORDS AND SPONGES |
FCI OPHTHALMICS, INC. |
K964774 |
10/22/1996 |
PUNCTUM PLUGS & READY-SET PUNCTAL PLUGS |
FCI OPHTHALMICS, INC. |
K955671 |
12/04/1995 |
RITLENG BICAN.LACR.SETS/SELF THREAD. MONOKAS(CHG.IN STER.) |
G.W.B. INTL., LTD. |
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