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 needle, conduction, anesthetic (w/wo introducer)
510(k) Number K894880
Device Name 16GA X 14 FOURTEEN LONG LONG BULLET POINT NEEDL
Applicant
R. J. DOYLE, INC.
P.O. BOX 278
SPIRIT LAKE,  ID  83869 -2179
Applicant Contact N HAMACHER,MD
Correspondent
R. J. DOYLE, INC.
P.O. BOX 278
SPIRIT LAKE,  ID  83869 -2179
Correspondent Contact N HAMACHER,MD
Regulation Number868.5150
Classification Product Code
BSP  
Date Received08/01/1989
Decision Date 11/30/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-