Last synced on 4 February 2023 at 10:33 pm

HEINE BETA 200(R) OPHTHALMOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131961
510(k) Type
Abbreviated
Applicant
HEINE OPTOTECHNIK GMBH & CO. KG.
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/4/2013
Days to Decision
160 days
Submission Type
Summary

HEINE BETA 200(R) OPHTHALMOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131961
510(k) Type
Abbreviated
Applicant
HEINE OPTOTECHNIK GMBH & CO. KG.
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/4/2013
Days to Decision
160 days
Submission Type
Summary