Last synced on 27 January 2023 at 11:04 pm

KEVOR-CURETTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882404
510(k) Type
Traditional
Applicant
EURO-MED INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1988
Days to Decision
28 days

KEVOR-CURETTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882404
510(k) Type
Traditional
Applicant
EURO-MED INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1988
Days to Decision
28 days