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DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052314
510(k) Type
Traditional
Applicant
DYNAREX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2005
Days to Decision
76 days
Submission Type
Summary

DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052314
510(k) Type
Traditional
Applicant
DYNAREX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2005
Days to Decision
76 days
Submission Type
Summary