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CHOLESTRON PRO II CHOLESTEROL TEST

Page Type
Cleared 510(K)
510(k) Number
K981345
510(k) Type
Traditional
Applicant
LIFESTREAM DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1998
Days to Decision
170 days
Submission Type
Summary

CHOLESTRON PRO II CHOLESTEROL TEST

Page Type
Cleared 510(K)
510(k) Number
K981345
510(k) Type
Traditional
Applicant
LIFESTREAM DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1998
Days to Decision
170 days
Submission Type
Summary