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DEX-CELL HYSTEROSCOPY FLUID DELIVERY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892001
510(k) Type
Traditional
Applicant
DEXIDE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1989
Days to Decision
80 days

DEX-CELL HYSTEROSCOPY FLUID DELIVERY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892001
510(k) Type
Traditional
Applicant
DEXIDE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1989
Days to Decision
80 days