Product code FRR
- Device name
- Chamber, Reverse Isolation, Patient Care
- Medical specialty
- General Hospital
- Device class
- 2
- Regulation number
- 880.5450
- Review panel
- HO
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- Y
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K922110 | GO-CLEAN | Viva-Tek Assoc., Inc. | 1994-03-09 |