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 Anesthesia Conduction Kit
510(k) Number K902312
Device Name COSPAN PEDIATRIC CONTINUOUS SPINAL ANESTHESIA TRAY
Applicant
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
2203 ALEXANDER ST.
SALT LAKE CITY,  UT  84119
Applicant Contact JOHN J VOZELLA
Correspondent
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
2203 ALEXANDER ST.
SALT LAKE CITY,  UT  84119
Correspondent Contact JOHN J VOZELLA
Regulation Number868.5140
Classification Product Code
CAZ  
Date Received05/23/1990
Decision Date 07/30/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-