LUMICON

Colorimeter, Photometer, Spectrophotometer For Clinical Use

The following data is part of a premarket notification filed by Hamilton Co. with the FDA for Lumicon.

Device ID	K873893
510k Number	K873893
Device Name:	LUMICON
Classification	Colorimeter, Photometer, Spectrophotometer For Clinical Use
Applicant	HAMILTON CO. POST OFFICE BOX 10030 Reno, NV 89520
Contact	Ken Lindner
Correspondent	Ken Lindner HAMILTON CO. POST OFFICE BOX 10030 Reno, NV 89520
Product Code	JJQ
CFR Regulation Number	862.2300 [🔎]
Decision	Substantially Equivalent (SESE)
Type	Traditional
3rd Party Reviewed	No
Combination Product	No
Date Received	1987-09-23
Decision Date	1988-01-05

Mark Image Registration \| Serial	Company Trademark Application Date
LUMICON 97511375 not registered Live/Pending	Advanced Opto-Mechanical Systems and Technologies Inc. 2022-07-20
LUMICON 87470828 not registered Live/Pending	Silicon Valley Optics Technology, Inc. 2017-05-31
LUMICON 87040344 not registered Dead/Abandoned	OPTICAL STRUCTURES INCORPORATED 2016-05-17
LUMICON 85719353 not registered Dead/Abandoned	LUMINATION LLC 2012-09-03
LUMICON 76975072 2867628 Dead/Cancelled	UMR Communications, Inc. 2000-10-13
LUMICON 76147544 2976556 Dead/Cancelled	UMR Communications, Inc. 2000-10-13
LUMICON 73649849 1531690 Dead/Cancelled	HAMILTON BONADUZ AG 1987-03-17
LUMICON 73286626 1238066 Dead/Cancelled	Marling; John B. 1980-11-20
LUMICON 72149121 0757726 Dead/Cancelled	PLASTIC CONTACT LENS COMPANY, THE 1962-07-16