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 withdrawal/infusion pump
510(k) Number K895688
Device Name NOBLES-LAI ENGINEERING INFUSION PUMP
Applicant
NOBLES-LAI ENGINEERING, INC.
3033 S. HARBOR BLVD.
SANTA ANA,  CA  92704
Applicant Contact NOBLES, PH.D
Correspondent
NOBLES-LAI ENGINEERING, INC.
3033 S. HARBOR BLVD.
SANTA ANA,  CA  92704
Correspondent Contact NOBLES, PH.D
Regulation Number870.1800
Classification Product Code
DQI  
Date Received09/22/1989
Decision Date 02/26/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-