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CATARACTSCREENER CT - S

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972440
510(k) Type
Traditional
Applicant
NEITZ INSTRUMENTS COMPANY, LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
9/30/1997
Days to Decision
92 days
Submission Type
Statement

CATARACTSCREENER CT - S

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972440
510(k) Type
Traditional
Applicant
NEITZ INSTRUMENTS COMPANY, LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
9/30/1997
Days to Decision
92 days
Submission Type
Statement