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 chair, ophthalmic, ac-powered
510(k) Number K863728
Device Name THE ERGOSYSTEM CHAIR
Applicant
CHARLES D. BELL, INC.
1214 RTE 130
WESTVILLE,  NJ  08093
Applicant Contact BELL, JR
Correspondent
CHARLES D. BELL, INC.
1214 RTE 130
WESTVILLE,  NJ  08093
Correspondent Contact BELL, JR
Regulation Number886.1140
Classification Product Code
HME  
Date Received09/23/1986
Decision Date 10/31/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-