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 Laparoscope, Gynecologic (And Accessories)
510(k) Number K852031
Device Name ENDOPORT 5MM
Applicant
Endotherapeutics
654 Bair Island Rd.
Suite 209
Redwood City,  CA  94063
Applicant Contact FREDERIC H MOLL
Correspondent
Endotherapeutics
654 Bair Island Rd.
Suite 209
Redwood City,  CA  94063
Correspondent Contact FREDERIC H MOLL
Regulation Number884.1720
Classification Product Code
HET  
Date Received05/09/1985
Decision Date 08/13/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-