Last synced on 20 December 2024 at 11:05 pm

ABDOMINAL SPATULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890374
510(k) Type
Traditional
Applicant
KINETIC MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1989
Days to Decision
11 days

ABDOMINAL SPATULA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890374
510(k) Type
Traditional
Applicant
KINETIC MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1989
Days to Decision
11 days