Last synced on 14 November 2025 at 11:06 pm

OPTUM(TM) AUTOMATED PATIENT ASSIST DEVICE

Page Type
Cleared 510(K)
510(k) Number
K883400
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1989
Days to Decision
476 days

OPTUM(TM) AUTOMATED PATIENT ASSIST DEVICE

Page Type
Cleared 510(K)
510(k) Number
K883400
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1989
Days to Decision
476 days