• 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 unit, electrosurgical and coagulation, with accessories
510(k) Number K873809
Device Name EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001
Applicant
ZIMMER ASPEN LABS
P.O. BOX 3936
ENGLEWOOD,  CO  80155
Applicant Contact JANE JOHNSON
Correspondent
ZIMMER ASPEN LABS
P.O. BOX 3936
ENGLEWOOD,  CO  80155
Correspondent Contact JANE JOHNSON
Regulation Number878.4400
Classification Product Code
BWA  
Date Received09/18/1987
Decision Date 11/20/1987
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
-
-