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 curette, uterine
510(k) Number K881794
Device Name IVORY FINDER SET
Applicant
IVORY INSTRUMENTS CO.
2447 W. 250TH ST.
LOMITA,  CA  90717
Applicant Contact EDWARD WALKER
Correspondent
IVORY INSTRUMENTS CO.
2447 W. 250TH ST.
LOMITA,  CA  90717
Correspondent Contact EDWARD WALKER
Regulation Number884.4530
Classification Product Code
HCY  
Date Received04/26/1988
Decision Date 07/08/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-