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SILICONE CATHETER REPAIR KITS

Page Type
Cleared 510(K)
510(k) Number
K926374
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
10/7/1994
Days to Decision
654 days
Submission Type
Statement

SILICONE CATHETER REPAIR KITS

Page Type
Cleared 510(K)
510(k) Number
K926374
510(k) Type
Traditional
Applicant
AKCESS MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
10/7/1994
Days to Decision
654 days
Submission Type
Statement