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 gas, calibration (specified concentration)
510(k) Number K870139
Device Name GAS, CALIBRATION, SPECIFIED CONCENTRATION
Applicant
PORTLAND WELDING SUPPLY, INC.
527 DANFORTH ST.
P.O. BOX 8361
PORTLAND,  ME  04104
Applicant Contact DIANE BRANSCOMB
Correspondent
PORTLAND WELDING SUPPLY, INC.
527 DANFORTH ST.
P.O. BOX 8361
PORTLAND,  ME  04104
Correspondent Contact DIANE BRANSCOMB
Regulation Number868.6400
Classification Product Code
BXK  
Date Received01/13/1987
Decision Date 02/10/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-