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IMPRA DUAL LUMEN SUBCLAVIAN - FEMORAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K883592
510(k) Type
Traditional
Applicant
IMPRA, INC.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
12/8/1988
Days to Decision
107 days

IMPRA DUAL LUMEN SUBCLAVIAN - FEMORAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K883592
510(k) Type
Traditional
Applicant
IMPRA, INC.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
12/8/1988
Days to Decision
107 days