Last synced on 14 November 2025 at 11:06 pm

BURTON KERATOMETER - MODLE 2040

Page Type
Cleared 510(K)
510(k) Number
K924779
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 KERATOMETER - MODLE 2040

Page Type
Cleared 510(K)
510(k) Number
K924779
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