Last synced on 14 November 2025 at 11:06 pm

SYMBION CENTRIFUGAL BLOOD PUMP MODEL I

Page Type
Cleared 510(K)
510(k) Number
K882129
510(k) Type
Traditional
Applicant
SYMBION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1988
Days to Decision
167 days

SYMBION CENTRIFUGAL BLOOD PUMP MODEL I

Page Type
Cleared 510(K)
510(k) Number
K882129
510(k) Type
Traditional
Applicant
SYMBION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1988
Days to Decision
167 days