Last synced on 14 November 2025 at 11:06 pm

ACCESS ULTRASENSITIVE HGH CALIBRATORS

Page Type
Cleared 510(K)
510(k) Number
K003098
510(k) Type
Traditional
Applicant
BECKMAN COULTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2000
Days to Decision
48 days
Submission Type
Summary

ACCESS ULTRASENSITIVE HGH CALIBRATORS

Page Type
Cleared 510(K)
510(k) Number
K003098
510(k) Type
Traditional
Applicant
BECKMAN COULTER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2000
Days to Decision
48 days
Submission Type
Summary