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SERIES 1500 DEFIBRILLATOR, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K926172
510(k) Type
Traditional
Applicant
MARQUETTE ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1993
Days to Decision
86 days
Submission Type
Summary

SERIES 1500 DEFIBRILLATOR, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K926172
510(k) Type
Traditional
Applicant
MARQUETTE ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1993
Days to Decision
86 days
Submission Type
Summary