Last synced on 14 November 2025 at 11:06 pm

ABUSCREEN CALIBRATION STANDARD

Page Type
Cleared 510(K)
510(k) Number
K932754
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1993
Days to Decision
55 days
Submission Type
Statement

ABUSCREEN CALIBRATION STANDARD

Page Type
Cleared 510(K)
510(k) Number
K932754
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1993
Days to Decision
55 days
Submission Type
Statement