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 analyzer, gas, oxygen, gaseous-phase
510(k) Number K852275
Device Name VASCULAR TECH # 100123 POLAROGRAPHIC OXGYEN SENSOR
Applicant
VASCULAR TECHNOLOGY INCORPORATED
MEDICAL DEVICE CONSULTANTS,INC
45 WEST STREET, SUITE 2
ATTLEBORO,  MA  02703
Applicant Contact WILLIAM A MORTON
Correspondent
VASCULAR TECHNOLOGY INCORPORATED
MEDICAL DEVICE CONSULTANTS,INC
45 WEST STREET, SUITE 2
ATTLEBORO,  MA  02703
Correspondent Contact WILLIAM A MORTON
Regulation Number868.1720
Classification Product Code
CCL  
Date Received05/29/1985
Decision Date 06/20/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-