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VISI-SPEAR EYE SPONGE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933872
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1993
Days to Decision
143 days
Submission Type
Summary

VISI-SPEAR EYE SPONGE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933872
510(k) Type
Traditional
Applicant
VISITEC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1993
Days to Decision
143 days
Submission Type
Summary