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COMEG ENDOSCOPY RESECTOSCOPE ACCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970764
510(k) Type
Traditional
Applicant
COMEG ENDOSCOPY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1997
Days to Decision
50 days
Submission Type
Summary

COMEG ENDOSCOPY RESECTOSCOPE ACCESSORIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970764
510(k) Type
Traditional
Applicant
COMEG ENDOSCOPY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1997
Days to Decision
50 days
Submission Type
Summary