FRR

Chamber, Reverse Isolation, Patient Care

Product code
FRR
Device name
Chamber, Reverse Isolation, Patient Care
Device class
Class 2
21 CFR
21 CFR 880.5450
Medical specialty
General Hospital
Marketing pathway
510(K)
Flag
Third-party review eligible
510(k) clearances (all years, FDA)
1 (all years; only the last 3 years are listed here)
Official FDA classification page: FRR
Classification and pathway per current FDA publications. Data from openFDA (CC0).