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AUTOREF LENSMETER RL-10

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925304
510(k) Type
Traditional
Applicant
CANON U.S.A., INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
2/17/1994
Days to Decision
484 days
Submission Type
Summary

AUTOREF LENSMETER RL-10

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925304
510(k) Type
Traditional
Applicant
CANON U.S.A., INC.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
2/17/1994
Days to Decision
484 days
Submission Type
Summary