510(k) K240256
- Device
- Remunity System
- Applicant
- Deka Research and Development
- 510(k) number
- K240256
- Product code
- QJY
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2024-06-12
- Date received
- 2024-01-31
- Regulation
- 880.5725
- Classification name
- Infusion Pump, Drug Specific, Pharmacy-Filled
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Related Records
Applicant Contact
- Contact
- Paul Smolenski
- Address
- 340 Commercial St. Manchester NH US 03101 03101
FDA Registration Numbers
- 1420032
- 3015192982
- 3016798778
- 1220973
- 1526534
- 1058584
- 2219920