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MODIFIED ACCESS R-CLONE ANA/RF SCREENING TEST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892421
510(k) Type
Traditional
Applicant
LIPOGEN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1989
Days to Decision
29 days

MODIFIED ACCESS R-CLONE ANA/RF SCREENING TEST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892421
510(k) Type
Traditional
Applicant
LIPOGEN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1989
Days to Decision
29 days