510(k) K831285

Device
Surgical/lid Margin Cover & Eyelash-
Applicant
RICHARD R. ANTHONY, M.D.
510(k) number
K831285
Product code
HOD
Decision
Substantially Equivalent (SESE)
Decision date
1983-06-03
Date received
1983-04-20
Regulation
886.4350
Classification name
Clamp, Eyelid, Ophthalmic
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HOD#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K924774BURTON AUTOMATIC PROJECTOR - MODEL CP-40R.H. Burton Co.1993-04-14
K891610HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENERKeeler Instruments, Inc.1989-06-05