Last synced on 30 September 2022 at 11:05 pm

NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURO-TRACE III NERVE BG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023342
510(k) Type
Traditional
Applicant
HDC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2004
Days to Decision
512 days
Submission Type
Summary

NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURO-TRACE III NERVE BG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023342
510(k) Type
Traditional
Applicant
HDC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2004
Days to Decision
512 days
Submission Type
Summary