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 table, obstetrical, ac-powered (and accessories)
510(k) Number K874610
Device Name ADEL MODEL 2100 BIRTHING BED
Applicant
ADEL MEDICAL LTD.
16700 S.E. 120TH AVE.
P.O. BOX 542
CLACKAMAS,  OR  97015
Applicant Contact MCCHORD
Correspondent
ADEL MEDICAL LTD.
16700 S.E. 120TH AVE.
P.O. BOX 542
CLACKAMAS,  OR  97015
Correspondent Contact MCCHORD
Regulation Number884.4900
Classification Product Code
HDD  
Date Received11/09/1987
Decision Date 01/21/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-