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GE MARQUETTE MEDICAL SYSTEMS PRUCKA CARDIOLAB CATH SYSTEM, VERSION 1.11

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000645
510(k) Type
Traditional
Applicant
GENERAL ELECTRIC MEDICAL SYSTEMS INFORMATION TECHN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/2000
Days to Decision
89 days
Submission Type
Summary

GE MARQUETTE MEDICAL SYSTEMS PRUCKA CARDIOLAB CATH SYSTEM, VERSION 1.11

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000645
510(k) Type
Traditional
Applicant
GENERAL ELECTRIC MEDICAL SYSTEMS INFORMATION TECHN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/24/2000
Days to Decision
89 days
Submission Type
Summary