Last synced on 14 November 2025 at 11:06 pm

IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST

Page Type
Cleared 510(K)
510(k) Number
K921968
510(k) Type
Traditional
Applicant
Tech-Co, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1996
Days to Decision
1523 days
Submission Type
Statement

IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST

Page Type
Cleared 510(K)
510(k) Number
K921968
510(k) Type
Traditional
Applicant
Tech-Co, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1996
Days to Decision
1523 days
Submission Type
Statement