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510(k) K873919

Device
TANGENT SCREEN
Applicant
RICHMOND PRODUCTS, INC.
510(k) number
K873919
Product code
HOJ  
Decision
Substantially Equivalent (SESE)
Decision date
1987-10-28
Date received
1987-09-25
Regulation
886.1810
Classification name
Screen, Tangent, Target
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 HOJ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K844657SPECTABLE FRAME MAGNIFYING BRILLETTEPro Design Intl. AS1984-12-11
K821081CHART PROJECTORMedical Equipment Designs, Inc.1982-06-14

Legacy Summary#

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FDA Review#

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