Last synced on 10 January 2025 at 11:05 pm

ACMI VISTA CTR BIPOLAR LOOP ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031001
510(k) Type
Special
Applicant
ACMI CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2003
Days to Decision
51 days
Submission Type
Summary

ACMI VISTA CTR BIPOLAR LOOP ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031001
510(k) Type
Special
Applicant
ACMI CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2003
Days to Decision
51 days
Submission Type
Summary