Last synced on 30 September 2022 at 11:05 pm

CEPHALOTOMY SCISSORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890388
510(k) Type
Traditional
Applicant
KINETIC MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1989
Days to Decision
21 days

CEPHALOTOMY SCISSORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890388
510(k) Type
Traditional
Applicant
KINETIC MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1989
Days to Decision
21 days