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 laryngoscope, rigid
510(k) Number K883296
Device Name LARYNGOSCOPE
Applicant
LOTHAR SCHARRAS
C/O REP GERMAN INDUSTRY/TRADE
ONE FARRAGUT SQUARE SOUTH N.W.
WASHINGTON,  DC  20006
Applicant Contact LOTHAR GRIESSBACH
Correspondent
LOTHAR SCHARRAS
C/O REP GERMAN INDUSTRY/TRADE
ONE FARRAGUT SQUARE SOUTH N.W.
WASHINGTON,  DC  20006
Correspondent Contact LOTHAR GRIESSBACH
Regulation Number868.5540
Classification Product Code
CCW  
Date Received08/04/1988
Decision Date 10/13/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-