Last synced on 16 May 2025 at 11:05 pm

OBJECTIVE REFRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802029
510(k) Type
Traditional
Applicant
ZEISS HUMPHREY SYSTEM
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
83 days

OBJECTIVE REFRACTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802029
510(k) Type
Traditional
Applicant
ZEISS HUMPHREY SYSTEM
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
83 days