FDA.reportPublic FDA data

510(k) K791988

Device
REPL. PISTON FOR TROUTMAN CORNEAL PUNCH
Applicant
EDWARD WECK, INC.
510(k) number
K791988
Product code
HNJ  
Decision
Substantially Equivalent (SESE)
Decision date
1979-10-30
Date received
1979-09-25
Regulation
886.4350
Classification name
Punch, Corneo-scleral
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 HNJ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K871646TANNE CORNEAL CUTTING BLOCKOcular Instruments, Inc.1987-05-18
K830335DORC CORNEAL PUNCH BLOCKJedmed Instrument Co.1983-03-09

Legacy Summary#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases

FDA Review#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases