Last synced on 10 January 2025 at 11:05 pm

ACMI BIPOLAR HEMOSTATIC SOURCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812637
510(k) Type
Traditional
Applicant
AMERICAN CYSTOCOPE MAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1981
Days to Decision
41 days

ACMI BIPOLAR HEMOSTATIC SOURCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812637
510(k) Type
Traditional
Applicant
AMERICAN CYSTOCOPE MAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1981
Days to Decision
41 days