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STIMUPLEX, NERVE STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K860126
510(k) Type
Traditional
Applicant
BURRON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1986
Days to Decision
45 days

STIMUPLEX, NERVE STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K860126
510(k) Type
Traditional
Applicant
BURRON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1986
Days to Decision
45 days