Last synced on 30 May 2025 at 11:05 pm

NEOCEPT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K811941
510(k) Type
Traditional
Applicant
ORGANON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1981
Days to Decision
21 days

NEOCEPT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K811941
510(k) Type
Traditional
Applicant
ORGANON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1981
Days to Decision
21 days