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510(k) K873915

Device
JACKSON CROSS CYLINDER TEST
Applicant
RICHMOND PRODUCTS, INC.
510(k) number
K873915
Product code
HOR  
Decision
Substantially Equivalent (SESE)
Decision date
1987-10-28
Date received
1987-09-25
Regulation
886.1840
Classification name
Simulatan (including Crossed Cylinder)
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

Legacy Summary#

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FDA Review#

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