The following data is part of a premarket notification filed by Covidien Llc with the FDA for Cytosponge Cell Collection Device.
| Device ID | K142695 |
| 510k Number | K142695 |
| Device Name: | Cytosponge Cell Collection Device |
| Classification | Esophagoscope (flexible Or Rigid) |
| Applicant | Covidien LLC 15 HAMPSHIRE ST Mansfield, MA 02048 |
| Contact | Richelle Hover |
| Correspondent | Richelle Hover Covidien LLC 15 HAMPSHIRE ST Mansfield, MA 02048 |
| Product Code | EOX |
| CFR Regulation Number | 874.4710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-09-22 |
| Decision Date | 2014-11-26 |
| Summary: | summary |