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 K954195
Device Name INDIGO PORTABLE LASER SYSTEM, INDDIGO FIBEROPTICS
Applicant
Indigo Medical, Inc.
1049 Elwell Ct.
Palo Alto,  CA  94303
Applicant Contact ALEX AXELROD
Correspondent
Indigo Medical, Inc.
1049 Elwell Ct.
Palo Alto,  CA  94303
Correspondent Contact ALEX AXELROD
Regulation Number878.4810
Classification Product Code
GEX  
Date Received09/06/1995
Decision Date 01/25/1996
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
-
-