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BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924778
510(k) Type
Traditional
Applicant
R.H. BURTON CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1993
Days to Decision
194 days
Submission Type
Statement

BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924778
510(k) Type
Traditional
Applicant
R.H. BURTON CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1993
Days to Decision
194 days
Submission Type
Statement