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 Electrosurgical, Cutting & Coagulation & Accessories
510(k) Number K885199
Device Name #500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES
Applicant
OLSEN ELECTROSURGICAL, INC.
2100 MERIDIAN PARK BLVD.
CONCORD,  CA  94520
Applicant Contact EUGENE OLSEN
Correspondent
OLSEN ELECTROSURGICAL, INC.
2100 MERIDIAN PARK BLVD.
CONCORD,  CA  94520
Correspondent Contact EUGENE OLSEN
Regulation Number878.4400
Classification Product Code
GEI  
Date Received12/16/1988
Decision Date 01/13/1989
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
Recalls CDRH Recalls
-
-