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 K903592
Device Name ESPI CLAW FORCEP, #8301, 5MM, 30 CM LENGTH
Applicant
DIXON MEDICAL, INC.
1534 S. JOHNSON FERRY RD.
ATLANTA,  GA  30319
Applicant Contact WILLIAM C DIXON
Correspondent
DIXON MEDICAL, INC.
1534 S. JOHNSON FERRY RD.
ATLANTA,  GA  30319
Correspondent Contact WILLIAM C DIXON
Regulation Number884.1720
Classification Product Code
HET  
Date Received08/08/1990
Decision Date 09/12/1990
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
-
-