Last synced on 25 January 2026 at 3:41 am

RAPIDHCG PREGNANCY TEST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981770
510(k) Type
Traditional
Applicant
Rapid Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1998
Days to Decision
17 days
Submission Type
Statement

RAPIDHCG PREGNANCY TEST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981770
510(k) Type
Traditional
Applicant
Rapid Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1998
Days to Decision
17 days
Submission Type
Statement