MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1998-03-03 for manufactured by .
| Report Number | 1811755-1998-00015 |
| MDR Report Key | 157998 |
| Report Source | 06 |
| Date Received | 1998-03-03 |
| Date of Event | 1998-02-02 |
| Date Mfgr Received | 1998-02-02 |
| Date Added to Maude | 1998-03-23 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 0 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Product Code | EMF |
| Date Received | 1998-03-03 |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Device Sequence No | 1 |
| Device Event Key | 153930 |
| Baseline Brand Name | KNIFELIGHT |
| Baseline Generic Name | KNIFE, SURGICAL LAMP, SURGICAL |
| Baseline Model No | 3300-001-000 |
| Baseline Catalog No | NA |
| Baseline ID | 3300-001-000 |
| Baseline Device Family | KNIFELIGHT |
| Baseline Shelf Life [Months] | NA |
| Baseline PMA Flag | N |
| Baseline 510K PMN | Y |
| Premarket Notification | K961122 |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1998-03-03 |