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IMPULSE EPIDURAL ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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