Last synced on 25 January 2026 at 3:41 am

ELISA TUBE PROLACTIN TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920921
510(k) Type
Traditional
Applicant
BIO CLINIC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/1992
Days to Decision
40 days
Submission Type
Statement

ELISA TUBE PROLACTIN TEST KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920921
510(k) Type
Traditional
Applicant
BIO CLINIC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/1992
Days to Decision
40 days
Submission Type
Statement