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UTERINE INJECTOR

Page Type
Cleared 510(K)
510(k) Number
K020292
510(k) Type
Traditional
Applicant
CATHETER RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2002
Days to Decision
79 days
Submission Type
Statement

UTERINE INJECTOR

Page Type
Cleared 510(K)
510(k) Number
K020292
510(k) Type
Traditional
Applicant
CATHETER RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/2002
Days to Decision
79 days
Submission Type
Statement