Emed Technologies Corporation
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 11
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K251105 | Tetra (TM-20); Tetra (TM-50) | December 22, 2025 |
| K240148 | SCIg60 Infusion System | February 16, 2024 |
| K230883 | VersaPump Infusion System | November 28, 2023 |
| K213429 | AccuSert Needle Inserter | October 20, 2022 |
| K222087 | SCIg60 Infusion System | October 13, 2022 |
| K173783 | SCIg60 Infusion System | December 14, 2018 |
| K161906 | SCIg60 Infuser | December 1, 2016 |
| K142319 | SCIg60 Infuser, Infuset | May 14, 2015 |
| K140133 | INFUSET FLOW CONTROL EXTENSION SET | May 15, 2014 |
| K140131 | SUB-Q SUBCUTANEOUS TISSUE INFUSION SET | April 3, 2014 |
| K123729 | VERSARATE FLOW RATE CONTROLER | December 21, 2012 |