Last synced on 14 November 2025 at 11:06 pm

ACCUSTROKE PIPET

Page Type
Cleared 510(K)
510(k) Number
K800141
510(k) Type
Traditional
Applicant
BECKMAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1980
Days to Decision
23 days

ACCUSTROKE PIPET

Page Type
Cleared 510(K)
510(k) Number
K800141
510(k) Type
Traditional
Applicant
BECKMAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1980
Days to Decision
23 days