• 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-machine, anesthesia
510(k) Number K131790
Device Name A9800 ANESTHESIA WORKSTATION
Applicant
ORICARE, INC.
1900 AM DRIVE
QUAKERTOWN,  PA  18951
Applicant Contact KURTIS MONTEGNA
Correspondent
ORICARE, INC.
1900 AM DRIVE
QUAKERTOWN,  PA  18951
Correspondent Contact KURTIS MONTEGNA
Regulation Number868.5160
Classification Product Code
BSZ  
Date Received06/18/2013
Decision Date 05/09/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-