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 K902962
Device Name LIFELOG(TM)
Applicant
MODULAR INSTRUMENTS, INC.
81 GREAT VALLEY PKWY.
MALVERN,  PA  19355
Applicant Contact LYNNE ARONSON
Correspondent
MODULAR INSTRUMENTS, INC.
81 GREAT VALLEY PKWY.
MALVERN,  PA  19355
Correspondent Contact LYNNE ARONSON
Regulation Number868.5160
Classification Product Code
BSZ  
Date Received07/05/1990
Decision Date 09/04/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-