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COLONOSCOPE GUIDING TUBE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884857
510(k) Type
Traditional
Applicant
MILL-ROSE LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/1989
Days to Decision
116 days

COLONOSCOPE GUIDING TUBE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884857
510(k) Type
Traditional
Applicant
MILL-ROSE LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/1989
Days to Decision
116 days