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NEITZ HALOGEN BINOCULAR INDIRECT OPHTHALMOSCOPE IO-A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942712
510(k) Type
Traditional
Applicant
NEITZ INSTRUMENTS COMPANY, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/1994
Days to Decision
57 days
Submission Type
Statement

NEITZ HALOGEN BINOCULAR INDIRECT OPHTHALMOSCOPE IO-A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942712
510(k) Type
Traditional
Applicant
NEITZ INSTRUMENTS COMPANY, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/1994
Days to Decision
57 days
Submission Type
Statement