Last synced on 14 November 2025 at 11:06 pm

CALIBRATOR

Page Type
Cleared 510(K)
510(k) Number
K915797
510(k) Type
Traditional
Applicant
ALKO DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1992
Days to Decision
37 days
Submission Type
Summary

CALIBRATOR

Page Type
Cleared 510(K)
510(k) Number
K915797
510(k) Type
Traditional
Applicant
ALKO DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1992
Days to Decision
37 days
Submission Type
Summary