Site Gills Style I/A Handpiece
FDA 510(k) K842459 · Chiron Vision Corp.
510(k) numberK842459
Submission
- Device name
- Site Gills Style I/A Handpiece
- Applicant
- Chiron Vision Corp.
Irvine, CA, US - Received
- June 22, 1984
- Decision date
- August 15, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Chiron Vision Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K970727 | Mport Foldable Lens Placement SystemMSS · Traditional | 12/17/1997SE |
| K972808 | Hansatome MicrokeratomeHNO · Traditional | 10/24/1997SE |
| K960414 | Synergist Power PackHQC · Traditional | 04/24/1996SE |
| K944993 | Iolab.Site CD Phacoemulsification ModuleHQC · Traditional | 10/12/1995SE |
| K944995 | Iolab/Site Peristaltic ModuleHQC · Traditional | 10/05/1995SE |
| K951292 | Passport Foldable Lens Placement SystemKYB · Traditional | 06/02/1995SE |
| K944994 | Iolab/Site Disposable Diaphragm CassetteHQC · Traditional | 03/14/1995SE |
| K941550 | Automatic Corneal Shaper Surgical InstrumentHNO · Traditional | 11/22/1994SE |
| K935233 | Iolab Lacrimal Duct CatheterOKS · Traditional | 09/15/1994SE |
| K925606 | Optical Zone/Hexagonal/Astigmatism/Radial MarkersHMR · Traditional | 08/29/1994SE |
Questions and answers
When was Site Gills Style I/A Handpiece cleared by the FDA?
Site Gills Style I/A Handpiece (K842459) received a 510(k) decision of Substantially Equivalent on August 15, 1984, 54 days after the submission was received.