Entarik Feeding Tube System; Entarik Feeding Tube— 510(k) K230206
Substantially EquivalentGravitas Medical, Inc.
FDA 510(k) clearance K230206 for Entarik Feeding Tube System; Entarik Feeding Tube, Substantially Equivalent on 2023-03-24. Applicant: Gravitas Medical, Inc..
Clearance details
- Applicant
- Gravitas Medical, Inc.
- Product code
- Code KNT
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Francisco, CA, US
Adverse events under product code KNT
product code KNT- Death
- 192
- Injury
- 6,034
- Malfunction
- 4,049
- Other
- 1
- Total
- 10,276
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.