Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Forceps, Ophthalmic
510(k) Number K843992
Device Name CILCOR OPHTHALMIC INSTRUMENTS
Applicant
Cilco, Inc.
1616 13th. Ave.
Suite 200
Huntington,  WV  25701
Applicant Contact RICK MCCARLEY
Correspondent
Cilco, Inc.
1616 13th. Ave.
Suite 200
Huntington,  WV  25701
Correspondent Contact RICK MCCARLEY
Regulation Number886.4350
Classification Product Code
HNR  
Date Received10/11/1984
Decision Date 11/21/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-