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COLONOSCOPIC INJECTION NEEDLE, C-323/C-325

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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