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 | Type | Status | Availability |
|---|---|---|---|
 Form FDA 3670 Medical Product Reporting Network (MedSun) |
Form and Instruction | Modified | Repair queued |
 0471_Supporting Statement B_2023.docx |
Supporting Statement B | Uploaded 2023-06-27 | Missing upstream |
| 0471_Supporting Statement A_2023.docx |
Supporting Statement A | Uploaded 2023-06-27 | Repair queued |
IC Document Collections
| IC ID | Collection | Type | Status | Form |
|---|---|---|---|---|
| 37668 |  Medical Product Reporting Network (MedSun) |
Form and Instruction | Modified |
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 |