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 extractor, vacuum, fetal
510(k) Number K963287
Device Name VACUUM CUP (004SD)
Applicant
SWIFT DELIVERY PRODUCTS
6824 ELK CANYON RD.
OKLAHOMA CITY,  OK  73162
Applicant Contact RICHARD G LINDSAY
Correspondent
SWIFT DELIVERY PRODUCTS
6824 ELK CANYON RD.
OKLAHOMA CITY,  OK  73162
Correspondent Contact RICHARD G LINDSAY
Regulation Number884.4340
Classification Product Code
HDB  
Date Received08/21/1996
Decision Date 10/28/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-