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MODIFICATION TO PAJUNK STIMULONG PLUS CATHETER SETS

Page Type
Cleared 510(K)
510(k) Number
K043130
510(k) Type
Special
Applicant
PAJUNK GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2004
Days to Decision
39 days
Submission Type
Summary

MODIFICATION TO PAJUNK STIMULONG PLUS CATHETER SETS

Page Type
Cleared 510(K)
510(k) Number
K043130
510(k) Type
Special
Applicant
PAJUNK GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2004
Days to Decision
39 days
Submission Type
Summary