Last synced on 30 September 2022 at 11:05 pm

PROBET (TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903002
510(k) Type
Traditional
Applicant
GYNOPHARMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1991
Days to Decision
270 days

PROBET (TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903002
510(k) Type
Traditional
Applicant
GYNOPHARMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1991
Days to Decision
270 days