EndoChoice Water Bottle Cap System— 510(k) K153588
Substantially EquivalentEndochoice, Inc.
FDA 510(k) clearance K153588 for EndoChoice Water Bottle Cap System, Substantially Equivalent on 2016-02-24. Applicant: Endochoice, Inc.. Device class: 2.
Clearance details
- Applicant
- Endochoice, Inc.
- Product code
- Code FEQ
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Alpharetta, GA, US
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More clearances from Endochoice, Inc.
view allAdverse events under product code FEQ
product code FEQ- Malfunction
- 1,135
- Total
- 1,135
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.