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 clamp, umbilical
510(k) Number K863645
Device Name SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000
Applicant
UNITED MEDICAL SYSTEMS, INC.
1901 E. CARNEGIE AVE.
SANTA ANA,  CA  92705
Applicant Contact GABRIEL DEUTSCH
Correspondent
UNITED MEDICAL SYSTEMS, INC.
1901 E. CARNEGIE AVE.
SANTA ANA,  CA  92705
Correspondent Contact GABRIEL DEUTSCH
Regulation Number884.4530
Classification Product Code
HFW  
Date Received09/18/1986
Decision Date 09/25/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-