Last synced on 25 January 2026 at 3:41 am

SYNELISA PROGESTERONE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933128
510(k) Type
Traditional
Applicant
ELIAS U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1993
Days to Decision
130 days
Submission Type
Statement

SYNELISA PROGESTERONE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933128
510(k) Type
Traditional
Applicant
ELIAS U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1993
Days to Decision
130 days
Submission Type
Statement