• 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 endoscope, neurological
510(k) Number K933244
Device Name DISPOSABLE GRASPING FORCEP
Applicant
NEURO NAVIGATIONAL CORP.
3180 PULLMAN ST.
COSTA MESA,  CA  92626
Applicant Contact KAREN U SALINAS
Correspondent
NEURO NAVIGATIONAL CORP.
3180 PULLMAN ST.
COSTA MESA,  CA  92626
Correspondent Contact KAREN U SALINAS
Regulation Number882.1480
Classification Product Code
GWG  
Date Received07/02/1993
Decision Date 09/10/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-