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 Airway, Nasopharyngeal
510(k) Number K901279
Device Name CHATHAM INDUSTRIES NASOPHARYNGEAL AIRWAY
Applicant
Chatham Industries
P.O. Box 324
Summit,  NJ  07901
Applicant Contact THOMAS K MURRAY
Correspondent
Chatham Industries
P.O. Box 324
Summit,  NJ  07901
Correspondent Contact THOMAS K MURRAY
Regulation Number868.5100
Classification Product Code
BTQ  
Date Received03/19/1990
Decision Date 03/28/1990
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
-
-