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COEURLOCK STERILE DISPOS. ANGIOGRAPHIC

Page Type
Cleared 510(K)
510(k) Number
K823920
510(k) Type
Traditional
Applicant
COEUR LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1983
Days to Decision
52 days

COEURLOCK STERILE DISPOS. ANGIOGRAPHIC

Page Type
Cleared 510(K)
510(k) Number
K823920
510(k) Type
Traditional
Applicant
COEUR LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1983
Days to Decision
52 days