FDA 510(k) Applications for Medical Device Product Code "MQU"
(Ocular Peg)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K980822 | FCI OPHTHALMICS, INC. | TITANIUM PEG SYSTEM | 07/09/1998 |
| K000151 | INTEGRATED ORBITAL IMPLANTS, INC. | PERRY-KOLBERG (PK) HA-COATED TITANIUM SLEEVE | 04/10/2000 |
| K974203 | INTEGRATED ORBITAL IMPLANTS, INC. | PERRY-KOLBERG (PK) TITANIUM MOTILITY/SUPPORT SYSTEM | 02/04/1998 |
| K971583 | POREX TECHNOLOGIES CORP. | MEDPOR OCULAR SCREW AND ACCEOSSORIES | 06/30/1997 |
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