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ACMI BIPOLAR RECTOSCOPE, MODEL EIWE-BR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021166
510(k) Type
Special
Applicant
ACMI-CIRCON CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2002
Days to Decision
28 days
Submission Type
Summary

ACMI BIPOLAR RECTOSCOPE, MODEL EIWE-BR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021166
510(k) Type
Special
Applicant
ACMI-CIRCON CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2002
Days to Decision
28 days
Submission Type
Summary