• 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 splint, nasal
510(k) Number K882244
Device Name RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT
Applicant
RICHARDS MEDICAL CO., INC.
1450 BROOKS RD.
MEMPHIS,  TN  38116
Applicant Contact ROBERT F GAMES
Correspondent
RICHARDS MEDICAL CO., INC.
1450 BROOKS RD.
MEMPHIS,  TN  38116
Correspondent Contact ROBERT F GAMES
Regulation Number874.5800
Classification Product Code
EPP  
Date Received05/31/1988
Decision Date 06/23/1988
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
-
-