FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Enteral Feeding Catheter
K Number: K202748
·
Decision Apr 9, 2021
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
5
Review Days
200
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Basic Information
- Device Name
- Enteral Feeding Catheter
- K Number
- K202748
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5980
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medcaptain Life Science Co., Ltd.
- Date Received
- September 21, 2020
- Decision Date
- April 9, 2021
- Product Code
- KNT
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KNT | Tubes, Gastrointestinal (And Accessories) | FDA class 2 | Gastroenterology, Urology |
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Other Clearances by Medcaptain Life Science Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K230528 | Extension Set | Dec 1, 2023 | Substantially Equivalent |
| K213004 | Needle Free Connector | May 10, 2022 | Substantially Equivalent |
| K202578 | KardiFlex NC Coronary Dilatation Catheter | May 6, 2021 | Substantially Equivalent |
| K202619 | KardiFlex PTCA Balloon Dilatation Catheter | Apr 29, 2021 | Substantially Equivalent |