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510(k) K862517

Device
BAUSCH & LOMB CONTACT LENS VIEWER
Applicant
BAUSCH & LOMB, INC.
510(k) number
K862517
Product code
HLF  
Decision
Substantially Equivalent (SESE)
Decision date
1986-08-11
Date received
1986-07-01
Regulation
886.1430
Classification name
Device, Measuring, Lens Radius, 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 HLF  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K930437MARCO STANDARD RADIUSGAUGESMarco Ophthalmic, Inc.1993-08-09
K823767ERG-JET ELECTRODELife-Tech Intl., Inc.1983-01-08

Legacy Summary#

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FDA Review#

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