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COMEG RESECTOSCOPE AND LASER-RESECTOSCOPE WORKING ELEMENTS/URETHROTOMES/ELECTRODES/ALBARRAB DEFLECTORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971881
510(k) Type
Traditional
Applicant
COMEG ENDOSCOPY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1997
Days to Decision
84 days
Submission Type
Summary

COMEG RESECTOSCOPE AND LASER-RESECTOSCOPE WORKING ELEMENTS/URETHROTOMES/ELECTRODES/ALBARRAB DEFLECTORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971881
510(k) Type
Traditional
Applicant
COMEG ENDOSCOPY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1997
Days to Decision
84 days
Submission Type
Summary