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IMPULSE EPIDURAL ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K884663
510(k) Type
Traditional
Applicant
IMPULSE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1989
Days to Decision
71 days

IMPULSE EPIDURAL ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K884663
510(k) Type
Traditional
Applicant
IMPULSE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1989
Days to Decision
71 days