• 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, electrosurgical
510(k) Number K884171
Device Name #875 DISPOSABLE BIOPOLAR CABLE
Applicant
OLSEN ELECTROSURGICAL, INC.
2100 MERIDIAN PARK BLVD.
CONCORD,  CA  94520
Applicant Contact EUGENE W OLSEN
Correspondent
OLSEN ELECTROSURGICAL, INC.
2100 MERIDIAN PARK BLVD.
CONCORD,  CA  94520
Correspondent Contact EUGENE W OLSEN
Regulation Number878.4400
Classification Product Code
HAM  
Date Received09/30/1988
Decision Date 10/24/1988
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
-
-