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LEOCOR GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K911270
510(k) Type
Traditional
Applicant
LEOCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1992
Days to Decision
301 days

LEOCOR GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K911270
510(k) Type
Traditional
Applicant
LEOCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1992
Days to Decision
301 days