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 K913489
Device Name SIEMENS MICRO2 PULSE OXIMETER
Applicant
SIEMENS MEDICAL ELECTRONICS
16 ELECTRONICS AVE.
DANVERS,  MA  01923
Applicant Contact ROBERT R MURFITT
Correspondent
SIEMENS MEDICAL ELECTRONICS
16 ELECTRONICS AVE.
DANVERS,  MA  01923
Correspondent Contact ROBERT R MURFITT
Regulation Number870.2700
Classification Product Code
DQA  
Date Received08/06/1991
Decision Date 10/30/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-