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 K962886
Device Name ANESTHESIA CONDUCTION NEEDLE
Applicant
ISPG, INC.
517 LITCHFIELD RD.
NEW MILFORD,  CT  06776
Applicant Contact LORETTA F LUHMAN
Correspondent
ISPG, INC.
517 LITCHFIELD RD.
NEW MILFORD,  CT  06776
Correspondent Contact LORETTA F LUHMAN
Regulation Number868.5150
Classification Product Code
BSP  
Date Received07/24/1996
Decision Date 10/09/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-