• 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 unit, examining/treatment, ent
510(k) Number K953457
Device Name JEDMED SPECTRUM ENT CABINET
Applicant
JEDMED INSTRUMENT CO.
5416 JEDMED CT.
ST. LOUIS,  MO  63129 -2221
Applicant Contact CRAIG R PARKS
Correspondent
JEDMED INSTRUMENT CO.
5416 JEDMED CT.
ST. LOUIS,  MO  63129 -2221
Correspondent Contact CRAIG R PARKS
Regulation Number874.5300
Classification Product Code
ETF  
Date Received07/21/1995
Decision Date 08/11/1995
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
-
-