• 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 K902611
Device Name I.C. MEDICAL SMOKE EVACUATOR ACTIVATOR
Applicant
I.C Medical, Inc.
2340 W. Shangri La
Suite 202
Phoenix,  AZ  85029
Applicant Contact A WILLARD
Correspondent
I.C Medical, Inc.
2340 W. Shangri La
Suite 202
Phoenix,  AZ  85029
Correspondent Contact A WILLARD
Regulation Number878.5070
Classification Product Code
FYD  
Date Received06/13/1990
Decision Date 08/17/1990
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
-
-