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)DeviceApplicantDecision date
K922110GO-CLEANViva-Tek Assoc., Inc.1994-03-09