K232594
- 510(k) number
- K232594
- Device name
- CATHTONG II PICC Catheter
- Applicant
- L&Z Us, Inc. NJ · US
- Product code
- LJS — Catheter, Intravascular, Therapeutic, Long-Term Grea
- Decision date
- 2023-09-22
- Date received
- 2023-08-25
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General Hospital
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K232594
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.