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360 SLX ADVISORY DEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K935922
510(k) Type
Traditional
Applicant
MEDICAL RESEARCH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1994
Days to Decision
374 days
Submission Type
Statement

360 SLX ADVISORY DEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K935922
510(k) Type
Traditional
Applicant
MEDICAL RESEARCH LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1994
Days to Decision
374 days
Submission Type
Statement