The following data is part of a premarket notification filed by Given Imaging Ltd. with the FDA for Modification To Given Diagnostic System.
| Device ID | K060805 |
| 510k Number | K060805 |
| Device Name: | MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM |
| Classification | System, Imaging, Esophageal, Wireless, Capsule |
| Applicant | GIVEN IMAGING LTD. SHAAR YOKNEAM NEW INDUSTRIAL ZONE, Yokneam (p.o.box 258), IL 20692 |
| Contact | Shoshana Friedman |
| Correspondent | Shoshana Friedman GIVEN IMAGING LTD. SHAAR YOKNEAM NEW INDUSTRIAL ZONE, Yokneam (p.o.box 258), IL 20692 |
| Product Code | NSI |
| CFR Regulation Number | 876.1300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-03-24 |
| Decision Date | 2006-05-24 |
| Summary: | summary |