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KERATOPLASTY SUTURING LENS

Page Type
Cleared 510(K)
510(k) Number
K802593
510(k) Type
Traditional
Applicant
PARIS CONTACT LENS LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1980
Days to Decision
62 days

KERATOPLASTY SUTURING LENS

Page Type
Cleared 510(K)
510(k) Number
K802593
510(k) Type
Traditional
Applicant
PARIS CONTACT LENS LABORATORY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1980
Days to Decision
62 days