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PE-3000 PULSE RATE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K854198
510(k) Type
Traditional
Applicant
QUANTUM LIFE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1986
Days to Decision
149 days

PE-3000 PULSE RATE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K854198
510(k) Type
Traditional
Applicant
QUANTUM LIFE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1986
Days to Decision
149 days