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MODIFICATION TO BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030332
510(k) Type
Special
Applicant
BIONICARE MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2003
Days to Decision
126 days
Submission Type
Summary

MODIFICATION TO BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030332
510(k) Type
Special
Applicant
BIONICARE MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2003
Days to Decision
126 days
Submission Type
Summary