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OPHTHALMIC KNIFE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922378
510(k) Type
Traditional
Applicant
MICROPTICS DEVELOPMENT LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/1992
Days to Decision
204 days
Submission Type
Summary

OPHTHALMIC KNIFE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922378
510(k) Type
Traditional
Applicant
MICROPTICS DEVELOPMENT LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/1992
Days to Decision
204 days
Submission Type
Summary