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 Shunt, Central Nervous System And Components
510(k) Number K792007
Device Name CSF-VENTRICULAR CATHETER, STANDARD DES
Applicant
PUDENZ-SCHULTE MEDICAL RESEARCH CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
PUDENZ-SCHULTE MEDICAL RESEARCH CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number882.5550
Classification Product Code
JXG  
Date Received10/05/1979
Decision Date 01/16/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-