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 System, Dialysate Delivery, Single Patient
510(k) Number K850179
Device Name MBM(TM) MONITRAL (R) BICARBONATE MODULE
Applicant
Hospal Medical Corp.
25 Kimberly Rd.
P.O. Box 857
East Brunswick,  NJ  08816
Applicant Contact JEAN-LOUIS FRESSINET
Correspondent
Hospal Medical Corp.
25 Kimberly Rd.
P.O. Box 857
East Brunswick,  NJ  08816
Correspondent Contact JEAN-LOUIS FRESSINET
Regulation Number876.5820
Classification Product Code
FKP  
Date Received01/17/1985
Decision Date 02/28/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-