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GASTROSCOPE AND COLONOSCOPE NOZZLE REPLACEMENT KITS

Page Type
Cleared 510(K)
510(k) Number
K970372
510(k) Type
Traditional
Applicant
PRECISION ENDOSCOPY OF AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1997
Days to Decision
39 days
Submission Type
Summary

GASTROSCOPE AND COLONOSCOPE NOZZLE REPLACEMENT KITS

Page Type
Cleared 510(K)
510(k) Number
K970372
510(k) Type
Traditional
Applicant
PRECISION ENDOSCOPY OF AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1997
Days to Decision
39 days
Submission Type
Summary