The following data is part of a premarket notification filed by Iridex Corp. with the FDA for Family Of Iris Medical Endoprobe Handpieces.
| Device ID | K022228 |
| 510k Number | K022228 |
| Device Name: | FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES |
| Classification | Powered Laser Surgical Instrument |
| Applicant | IRIDEX CORP. 1212 TERRA BELLA AVE. Mountain View, CA 94043 |
| Contact | John D'angelo |
| Correspondent | John D'angelo IRIDEX CORP. 1212 TERRA BELLA AVE. Mountain View, CA 94043 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-07-10 |
| Decision Date | 2002-10-08 |
| Summary: | summary |