The following data is part of a premarket notification filed by Endochoice, Inc. with the FDA for Endochoice Water Bottle Cap System.
Device ID | K142155 |
510k Number | K142155 |
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 | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-08-06 |
Decision Date | 2015-01-20 |
Summary: | summary |