Brand Name | CLASSIC HYPERBARIC |
Type of Device | CHAMBER, HYPERBARIC |
MDR Report Key | 15283211 |
MDR Text Key | 298705438 |
Report Number | MW5111688 |
Device Sequence Number | 1 |
Product Code |
CBF
|
Combination Product (y/n) | N |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Voluntary
|
Reporter Occupation |
Unknown
|
Type of Report
| Initial |
Report Date |
08/20/2022 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
Not provided |
Initial Date FDA Received | 08/23/2022 |
Patient Sequence Number | 1 |
|
|