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CARDIOCATH CATHETERIZATION LAB SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K960321
510(k) Type
Traditional
Applicant
PRUCKA ENGINEERING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1996
Days to Decision
212 days
Submission Type
Summary

CARDIOCATH CATHETERIZATION LAB SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K960321
510(k) Type
Traditional
Applicant
PRUCKA ENGINEERING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/1996
Days to Decision
212 days
Submission Type
Summary