The following data is part of a premarket notification filed by Endochoice, Inc. with the FDA for Endochoice Water Bottle Cap System.
| Device ID | K153588 |
| 510k Number | K153588 |
| Device Name: | EndoChoice Water Bottle Cap System |
| Classification | Pump, Air, Non-manual, For Endoscope |
| Applicant | ENDOCHOICE, INC. 11810 WILLS RD. Alpharetta, GA 30009 |
| Contact | Daniel Hoefer |
| Correspondent | Daniel Hoefer ENDOCHOICE, INC. 11810 WILLS RD. Alpharetta, GA 30009 |
| Product Code | FEQ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-12-16 |
| Decision Date | 2016-02-24 |
| Summary: | summary |