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 Circuit, Breathing (W Connector, Adaptor, Y Piece)
510(k) Number K833478
Device Name HUMPHREY A.D.E. SYSTEM
Applicant
ANAESTHETIC BREATHING SYSTEM
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
ANAESTHETIC BREATHING SYSTEM
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number868.5240
Classification Product Code
CAI  
Date Received10/24/1983
Decision Date 12/16/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-