• 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 laryngoscope, nasopharyngoscope
510(k) Number K831255
Device Name LARYNGOSCOPE ATTACHMENT PH2000
Applicant
EDER INSTRUMENT CO, INC.
735 NORTH WATER ST.
SUITE 1102
MILWAUKEE, WI 53202,  53202
Correspondent
EDER INSTRUMENT CO, INC.
735 NORTH WATER ST.
SUITE 1102
MILWAUKEE, WI 53202,  53202
Regulation Number874.4760
Classification Product Code
EQN  
Date Received04/18/1983
Decision Date 09/12/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-