BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR

Projector, Ophthalmic

BAUSCH & LOMB, INC.

The following data is part of a premarket notification filed by Bausch & Lomb, Inc. with the FDA for Bausch & Lomb Accu-chart 3 Acuity Projector.

Pre-market Notification Details

Device IDK862519
510k NumberK862519
Device Name:BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR
ClassificationProjector, Ophthalmic
Applicant BAUSCH & LOMB, INC. 1400 NORTH GOODMAN ST. P.O.BOX 450 Rochester,  NY  14692
ContactNicholas A Walp
CorrespondentNicholas A Walp
BAUSCH & LOMB, INC. 1400 NORTH GOODMAN ST. P.O.BOX 450 Rochester,  NY  14692
Product CodeHOS  
CFR Regulation Number886.1680 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-07-01
Decision Date1986-07-23

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.