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AEDEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K002232
510(k) Type
Traditional
Applicant
MEDICAL RESEARCH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2000
Days to Decision
135 days
Submission Type
Statement

AEDEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K002232
510(k) Type
Traditional
Applicant
MEDICAL RESEARCH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2000
Days to Decision
135 days
Submission Type
Statement