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KERATOME BLADE 200200 & 600600

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020482
510(k) Type
Traditional
Applicant
MICROSPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2002
Days to Decision
306 days
Submission Type
Summary

KERATOME BLADE 200200 & 600600

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020482
510(k) Type
Traditional
Applicant
MICROSPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2002
Days to Decision
306 days
Submission Type
Summary