• 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 K942130
Device Name M.A.G. INC. MAPLESON D CIRCUITS
Applicant
MAG, INC.
30 ROBB HILL RD.
MARTINSVILLE,  IN  46151
Applicant Contact ROB FYE
Correspondent
MAG, INC.
30 ROBB HILL RD.
MARTINSVILLE,  IN  46151
Correspondent Contact ROB FYE
Regulation Number868.5240
Classification Product Code
CAI  
Date Received05/03/1994
Decision Date 06/22/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-