Last synced on 14 November 2025 at 11:06 pm

THIRD GENERATION PSA CONTROL MODULE

Page Type
Cleared 510(K)
510(k) Number
K981455
510(k) Type
Special
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/1998
Days to Decision
20 days
Submission Type
Summary

THIRD GENERATION PSA CONTROL MODULE

Page Type
Cleared 510(K)
510(k) Number
K981455
510(k) Type
Special
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/1998
Days to Decision
20 days
Submission Type
Summary