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510(k) K874250

Device
THREE CHAR. TEST-CHILD & WORTH 4 DOT TEST NEARPT.
Applicant
RICHMOND PRODUCTS, INC.
510(k) number
K874250
Product code
HLP  
Decision
Substantially Equivalent (SESE)
Decision date
1988-01-11
Date received
1987-10-19
Regulation
886.1880
Classification name
Target, Fusion And Stereoscopic
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
LLOYD POWELL
Address
1021 So Rogers Cir. Boca Raton FL US 33487 33487

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HLP  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K883471VKG 1000, VIDEO KERATOMETERTechnitex, Inc.1988-11-08
K874251WORTH 4 DOT TEST DISTANCE C/W MUSCLE LIGHTRichmond Products, Inc.1988-01-11

Legacy Summary#

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FDA Review#

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