The following data is part of a premarket notification filed by Draeger Medical Systems, Inc. with the FDA for Isolette 8000 Plus.
| Device ID | K182977 |
| 510k Number | K182977 |
| Device Name: | Isolette 8000 Plus |
| Classification | Incubator, Neonatal |
| Applicant | Draeger Medical Systems, Inc. 3135 Quarry Road Telford, PA 18969 |
| Contact | Karen Otrupchak |
| Correspondent | Karen Otrupchak Draeger Medical Systems, Inc. 3135 Quarry Road Telford, PA 18969 |
| Product Code | FMZ |
| CFR Regulation Number | 880.5400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-10-26 |
| Decision Date | 2018-11-21 |
| Summary: | summary |