FDA 510(k)
FDA class 2
Unknown
🇺🇸 United States
Hemodialysis Catheter
K Number: K241581
·
Decision May 16, 2025
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
123
Applicant Total
3
Review Days
347
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Basic Information
- Device Name
- Hemodialysis Catheter
- K Number
- K241581
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5540
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Unknown
- Statement or Summary
- Summary
- Applicant
- Haolang Medical USA Corporation
- Date Received
- June 3, 2024
- Decision Date
- May 16, 2025
- Product Code
- MSD
- 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 |
|---|---|---|---|
| MSD | Catheter, Hemodialysis, Implanted | FDA class 2 | Gastroenterology, Urology |
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