Last synced on 2 May 2025 at 11:05 pm

IN-VITRO DIAGNOSTIC VAGINITIS TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050352
510(k) Type
Traditional
Applicant
AMERITEK RESEARCH LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2005
Days to Decision
202 days
Submission Type
Statement

IN-VITRO DIAGNOSTIC VAGINITIS TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050352
510(k) Type
Traditional
Applicant
AMERITEK RESEARCH LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2005
Days to Decision
202 days
Submission Type
Statement