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 Catheters, Suction, Tracheobronchial
510(k) Number K903669
Device Name GENESIS INSUFFLATING CATHETER
Applicant
General Medical Co.
400 Interstate N. Pkwy.
Suite 650
Atlanta,  GA  30339
Applicant Contact JOHN SELLERS
Correspondent
General Medical Co.
400 Interstate N. Pkwy.
Suite 650
Atlanta,  GA  30339
Correspondent Contact JOHN SELLERS
Regulation Number868.6810
Classification Product Code
BSY  
Date Received08/13/1990
Decision Date 09/12/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-