The following data is part of a premarket notification filed by Richmond Products, Inc. with the FDA for Jackson Cross Cylinder Test.
Device ID | K873915 |
510k Number | K873915 |
Device Name: | JACKSON CROSS CYLINDER TEST |
Classification | Simulatan (including Crossed Cylinder) |
Applicant | RICHMOND PRODUCTS, INC. 1021 SO ROGERS CIRCLE Boca Raton, FL 33487 -2894 |
Contact | Lloyd Powell |
Correspondent | Lloyd Powell RICHMOND PRODUCTS, INC. 1021 SO ROGERS CIRCLE Boca Raton, FL 33487 -2894 |
Product Code | HOR |
CFR Regulation Number | 886.1840 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-09-25 |
Decision Date | 1987-10-28 |