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BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012018
510(k) Type
Traditional
Applicant
ACMI CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2002
Days to Decision
383 days
Submission Type
Summary

BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012018
510(k) Type
Traditional
Applicant
ACMI CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2002
Days to Decision
383 days
Submission Type
Summary