Last synced on 30 May 2025 at 11:05 pm

PREG-BETA ONE HOUR TUBE TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841853
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1984
Days to Decision
50 days

PREG-BETA ONE HOUR TUBE TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841853
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1984
Days to Decision
50 days