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-machine, anesthesia
510(k) Number K854213
Device Name ARI STANDARD ANESTHESIA RECORD
Applicant
AGILENT TECHNOLOGIES, INC.
1500 OLIVER BUILDING
PITTSBURGH,  PA  15222
Applicant Contact EDWARD WEISGERBER
Correspondent
AGILENT TECHNOLOGIES, INC.
1500 OLIVER BUILDING
PITTSBURGH,  PA  15222
Correspondent Contact EDWARD WEISGERBER
Regulation Number868.5160
Classification Product Code
BSZ  
Date Received10/17/1985
Decision Date 12/19/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-