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ANGIOMAT 3000, 6000, CT INJECTOR

Page Type
Cleared 510(K)
510(k) Number
K944875
510(k) Type
Traditional
Applicant
LIEVEL-FLARSHEIM CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1995
Days to Decision
93 days
Submission Type
Statement

ANGIOMAT 3000, 6000, CT INJECTOR

Page Type
Cleared 510(K)
510(k) Number
K944875
510(k) Type
Traditional
Applicant
LIEVEL-FLARSHEIM CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1995
Days to Decision
93 days
Submission Type
Statement