Last synced on 21 June 2024 at 11:04 pm

MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990379
510(k) Type
Special
Applicant
DEXIDE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1999
Days to Decision
24 days
Submission Type
Summary