Last synced on 14 November 2025 at 11:06 pm

LEMPERT OPTIC DISC ANALYSIS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K923708
510(k) Type
Traditional
Applicant
LEMPERT OPHTHALMIC INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1993
Days to Decision
235 days
Submission Type
Statement

LEMPERT OPTIC DISC ANALYSIS SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K923708
510(k) Type
Traditional
Applicant
LEMPERT OPHTHALMIC INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1993
Days to Decision
235 days
Submission Type
Statement