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INTRAVENOUS CATHETERS MODIFICATIONS

Page Type
Cleared 510(K)
510(k) Number
K921295
510(k) Type
Traditional
Applicant
CRITIKON COMPANY,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1993
Days to Decision
431 days
Submission Type
Summary

INTRAVENOUS CATHETERS MODIFICATIONS

Page Type
Cleared 510(K)
510(k) Number
K921295
510(k) Type
Traditional
Applicant
CRITIKON COMPANY,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1993
Days to Decision
431 days
Submission Type
Summary