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BKS-1000 REFRACTIVE SET USE IN KERATOREFRACTIVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870807
510(k) Type
Traditional
Applicant
ALLERGAN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/1987
Days to Decision
91 days

BKS-1000 REFRACTIVE SET USE IN KERATOREFRACTIVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K870807
510(k) Type
Traditional
Applicant
ALLERGAN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/1987
Days to Decision
91 days