• 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 illuminator, fiberoptic, surgical field
510(k) Number K882956
Device Name VITAL-VUE ILLUMINATION, SUCTION AND IRRIGATION
Applicant
VITALMETRICS, INC.
1150 17TH STREET, N.W.
SUITE 1000
WASHINGTON,  DC  20036
Applicant Contact JOHN B DUBECK
Correspondent
VITALMETRICS, INC.
1150 17TH STREET, N.W.
SUITE 1000
WASHINGTON,  DC  20036
Correspondent Contact JOHN B DUBECK
Regulation Number878.4580
Classification Product Code
HBI  
Date Received07/13/1988
Decision Date 08/03/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-