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 Apparatus, Exhaust, Surgical
510(k) Number K896822
Device Name SURGISMOKE
Applicant
SPECTRO INDUSTRIES, INC.
1794 MAPLE LN.
ROSEVILLE,  MN  55113
Applicant Contact DONALD HEWITT
Correspondent
SPECTRO INDUSTRIES, INC.
1794 MAPLE LN.
ROSEVILLE,  MN  55113
Correspondent Contact DONALD HEWITT
Regulation Number878.5070
Classification Product Code
FYD  
Date Received12/04/1989
Decision Date 01/11/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-