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 Spatula, Cervical, Cytological
510(k) Number K915844
Device Name EXACT-TOUCH
Applicant
Baal Assoc., Inc.
P.O. Box 571273
Salt Lake City,  UT  84107
Applicant Contact LARRY E PAGE
Correspondent
Baal Assoc., Inc.
P.O. Box 571273
Salt Lake City,  UT  84107
Correspondent Contact LARRY E PAGE
Regulation Number884.4530
Classification Product Code
HHT  
Date Received12/26/1991
Decision Date 01/07/1994
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
-
-