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, Radiographic, Stationary Top
510(k) Number K893690
Device Name SUPER SPEED POTTER-BUCKY (ESO5-110 & 220)
Applicant
Hofmann X-Ray of America, Inc.
16540 Aston St.
Irvine,  CA  92714
Applicant Contact ROBERT DOUBLEDEE
Correspondent
Hofmann X-Ray of America, Inc.
16540 Aston St.
Irvine,  CA  92714
Correspondent Contact ROBERT DOUBLEDEE
Regulation Number892.1980
Classification Product Code
IXQ  
Date Received05/16/1989
Decision Date 07/20/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-