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CATARACT DIAMOND KNIFE

Page Type
Cleared 510(K)
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)
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