| Device Type ID | 2575 |
| Device Name | Pad, Neonatal Eye |
| Regulation Description | Neonatal Eye Pad. |
| Regulation Medical Specialty | General Hospital |
| Review Panel | General Hospital |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Anesthesiology, General Hospital, Infection Control, And Dental Devices (DAGRID) General Hospital Devices Branch (GHDB) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 880.5270 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | FOK |
| GMP Exempt | Yes |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 2575 |
| Device | Pad, Neonatal Eye |
| Product Code | FOK |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Neonatal Eye Pad. |
| CFR Regulation Number | 880.5270 [🔎] |
| Device Problems | |
|---|---|
Device Emits Odor | 5 |
Use Of Device Problem | 4 |
Improper Or Incorrect Procedure Or Method | 2 |
| Total Device Problems | 11 |