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510(k) K862519

Device
BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR
Applicant
BAUSCH & LOMB, INC.
510(k) number
K862519
Product code
HOS  
Decision
Substantially Equivalent (SESE)
Decision date
1986-07-23
Date received
1986-07-01
Regulation
886.1680
Classification name
Projector, Ophthalmic
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
NICHOLAS A WALP
Address
1400 N. Goodman St. P.O.Box 450 Rochester NY US 14692 14692

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HOS  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K936200WIRELESS CHART PROJECTOR,HCP-W 721Canon USA, Inc.1994-09-28
K930443MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJEMarco Ophthalmic, Inc.1993-07-06
K924784BURTON PROJECTOR HEAD - MODEL 6000-HR.H. Burton Co.1993-04-05
K921214OPHTHALMIC PROJECTORLuneau Ophtalmologie SA1992-06-11
K890992WOODLYN OPHTHALMIC PROJECTORWoodlyn, Inc.1989-05-17
K812706MILLER/NADLER GLARE TESTERMosebach Electric & Supply1981-11-16
K811180ULTRAMATIC PROJECT-O-CHART OPHTH. PROJAmerican Optical Corp.1981-05-15
K781658PROJECTOR, ACCU-CHART ACUITYBausch & Lomb, Inc.1978-10-17

Legacy Summary#

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FDA Review#

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