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PULSELIFE STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K840983
510(k) Type
Traditional
Applicant
PULSE LIFE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1984
Days to Decision
21 days

PULSELIFE STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K840983
510(k) Type
Traditional
Applicant
PULSE LIFE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1984
Days to Decision
21 days