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 oximeter
510(k) Number K914620
Device Name HMS-4000 PHYSIOLOGICAL MONITOR, MODIFICATION
Applicant
VITALOG MONITORING,INC.
643 BAIR ISLAND RD.,STE.300
REDWOOD CITY,  CA  94063
Applicant Contact LAUGHTON E MILES
Correspondent
VITALOG MONITORING,INC.
643 BAIR ISLAND RD.,STE.300
REDWOOD CITY,  CA  94063
Correspondent Contact LAUGHTON E MILES
Regulation Number870.2700
Classification Product Code
DQA  
Date Received10/16/1991
Decision Date 05/01/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-