Last synced on 14 November 2025 at 11:06 pm

ABBOTT PATIENT ASSIST DEVICE

Page Type
Cleared 510(K)
510(k) Number
K830766
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1983
Days to Decision
19 days

ABBOTT PATIENT ASSIST DEVICE

Page Type
Cleared 510(K)
510(k) Number
K830766
510(k) Type
Traditional
Applicant
ABBOTT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1983
Days to Decision
19 days