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CATARACT DIAMOND KNIFE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863725
510(k) Type
Traditional
Applicant
MEDICAL TECHNOLOGY DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/1986
Days to Decision
38 days

CATARACT DIAMOND KNIFE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K863725
510(k) Type
Traditional
Applicant
MEDICAL TECHNOLOGY DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/1986
Days to Decision
38 days