• 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 Electrosurgical, Cutting & Coagulation & Accessories
510(k) Number K060183
Device Name ERBE APC INTEGRATED FILTER PROBES; ERBE APC INTEGRATED FILTER PROBE ADAPTER
Applicant
Erbe USA, Inc.
2225 Northwest Pkwy.
Marietta,  GA  30157
Applicant Contact JOHN TARTAL
Correspondent
Erbe USA, Inc.
2225 Northwest Pkwy.
Marietta,  GA  30157
Correspondent Contact JOHN TARTAL
Regulation Number878.4400
Classification Product Code
GEI  
Date Received01/24/2006
Decision Date 02/16/2006
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-