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PLANCON MIRCOLAMELLAR KERATOME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960395
510(k) Type
Traditional
Applicant
PLANCON INSTRUMENTS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/26/1996
Days to Decision
88 days
Submission Type
Summary

PLANCON MIRCOLAMELLAR KERATOME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960395
510(k) Type
Traditional
Applicant
PLANCON INSTRUMENTS
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/26/1996
Days to Decision
88 days
Submission Type
Summary