Last synced on 14 November 2025 at 11:06 pm

TRIONOMER

Page Type
Cleared 510(K)
510(k) Number
K022150
510(k) Type
Traditional
Applicant
PENTRON CLINICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2002
Days to Decision
50 days
Submission Type
Summary

TRIONOMER

Page Type
Cleared 510(K)
510(k) Number
K022150
510(k) Type
Traditional
Applicant
PENTRON CLINICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2002
Days to Decision
50 days
Submission Type
Summary