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MITYVIEW 4-WAY LATERAL EXPANDER SPECULUM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000444
510(k) Type
Traditional
Applicant
Prism Enterprises, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2000
Days to Decision
71 days
Submission Type
Summary

MITYVIEW 4-WAY LATERAL EXPANDER SPECULUM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000444
510(k) Type
Traditional
Applicant
Prism Enterprises, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2000
Days to Decision
71 days
Submission Type
Summary