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ACUVANCE PLUS SAFETY IV CATHETER, PROTECTIV PLUS SAFETY IV CATHETER, OPTIVA IV CATHETER

Page Type
Cleared 510(K)
510(k) Number
K030571
510(k) Type
Traditional
Applicant
ETHICON ENDO-SURGERY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2003
Days to Decision
32 days
Submission Type
Summary

ACUVANCE PLUS SAFETY IV CATHETER, PROTECTIV PLUS SAFETY IV CATHETER, OPTIVA IV CATHETER

Page Type
Cleared 510(K)
510(k) Number
K030571
510(k) Type
Traditional
Applicant
ETHICON ENDO-SURGERY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2003
Days to Decision
32 days
Submission Type
Summary