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DISPOSABLE NERVE STIMULATING PROBE, BIPOLAR CONCENTRIC, DISPOSABLE NERVE STIMULATOR PROBE, BIPOLAR SIDE BY SIDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100912
510(k) Type
Traditional
Applicant
Kirwan Surgical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2010
Days to Decision
140 days
Submission Type
Summary

DISPOSABLE NERVE STIMULATING PROBE, BIPOLAR CONCENTRIC, DISPOSABLE NERVE STIMULATOR PROBE, BIPOLAR SIDE BY SIDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100912
510(k) Type
Traditional
Applicant
Kirwan Surgical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2010
Days to Decision
140 days
Submission Type
Summary