Last synced on 25 January 2026 at 3:41 am

COLONOSCOPIC INJECTION NEEDLE, C-323/C-325

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921800
510(k) Type
Traditional
Applicant
MILL-ROSE LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1993
Days to Decision
300 days
Submission Type
Statement

COLONOSCOPIC INJECTION NEEDLE, C-323/C-325

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921800
510(k) Type
Traditional
Applicant
MILL-ROSE LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1993
Days to Decision
300 days
Submission Type
Statement