Last synced on 14 November 2025 at 11:06 pm

NON-STERILE,SINGLE/SOUBLE LUMEN-CATH

Page Type
Cleared 510(K)
510(k) Number
K830233
510(k) Type
Traditional
Applicant
EVERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1983
Days to Decision
34 days

NON-STERILE,SINGLE/SOUBLE LUMEN-CATH

Page Type
Cleared 510(K)
510(k) Number
K830233
510(k) Type
Traditional
Applicant
EVERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1983
Days to Decision
34 days