Information Collection Request
Adverse Event Program for Medical Devices (Medical Product Safety Network (MedSun))
ICR 202212-0910-005 · OMB 0910-0471 · Received in OIRA
Forms and Documents
Document Name | Status |
|---|---|
Form and Instruction |
Modified |
Supporting Statement B | 2023-06-27 |
Supporting Statement A | 2023-06-27 |
Form FDA 3670 Medical Product Reporting Network (MedSun)
0471_Supporting Statement B_2023.docxIC Document Collections
| IC ID | Document Title | Status | |
|---|---|---|---|
| 37668 | Modified |
Medical Product Reporting Network (MedSun)ICR Details
| Status | Received in OIRA |
|---|---|
| Agency/Subagency | HHS/FDA |
| OMB Control No | 0910-0471 |
| Type of Information Collection | Extension without change of a currently approved collection |
| Previous ICR Reference No | 202005-0910-012 |
| Agency Tracking No | CDRH |
| Date Submitted to OIRA | 1969-12-31 |
| Requested Expiration Date | 1969-12-31 |