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 Transport, Patient, Powered
510(k) Number K923912
Device Name MOORE MANUFACTURE MODEL-MHBTL
Applicant
Moore Mfg., Inc.
1505 N. Locust St.
Canby,  OR  97013
Applicant Contact ARNOLD L MOORE
Correspondent
Moore Mfg., Inc.
1505 N. Locust St.
Canby,  OR  97013
Correspondent Contact ARNOLD L MOORE
Regulation Number890.5150
Classification Product Code
ILK  
Date Received08/04/1992
Decision Date 02/12/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-