Last synced on 30 September 2022 at 11:05 pm

STREAK RETINOSCOPE RX-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950789
510(k) Type
Traditional
Applicant
NEITZ INSTRUMENTS COMPANY, LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
3/28/1995
Days to Decision
35 days
Submission Type
Statement

STREAK RETINOSCOPE RX-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950789
510(k) Type
Traditional
Applicant
NEITZ INSTRUMENTS COMPANY, LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
3/28/1995
Days to Decision
35 days
Submission Type
Statement