• 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 tube, tracheal (w/wo connector)
510(k) Number K925508
Device Name RUSCH SAFETY CLEAR PLUS CUFFED W/MAGILL TIP
Applicant
RUSCH, INC.
TALL PINES PARK
JAFFREY,  NH  03452
Applicant Contact RICHARD T LYKINS
Correspondent
RUSCH, INC.
TALL PINES PARK
JAFFREY,  NH  03452
Correspondent Contact RICHARD T LYKINS
Regulation Number868.5730
Classification Product Code
BTR  
Date Received11/09/1992
Decision Date 09/02/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-