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 Powered Laser Surgical Instrument
510(k) Number K844178
Device Name MODEL TT25RF
Applicant
Inframed, Inc.
P.O. Box 761
Brookline Village,  MA  02147
Applicant Contact RAYMOND F FENNESSEY
Correspondent
Inframed, Inc.
P.O. Box 761
Brookline Village,  MA  02147
Correspondent Contact RAYMOND F FENNESSEY
Regulation Number878.4810
Classification Product Code
GEX  
Date Received10/26/1984
Decision Date 10/18/1985
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
Predetermined Change
Control Plan Authorized		 No
-
-