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GASTROSCOPE AND COLONOSCOPE NOZZLE REPLACEMENT KITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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