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Bi-Blade Vitrectomy Cutter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153168
510(k) Type
Special
Applicant
MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2016
Days to Decision
179 days
Submission Type
Summary

Bi-Blade Vitrectomy Cutter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153168
510(k) Type
Special
Applicant
MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2016
Days to Decision
179 days
Submission Type
Summary