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 processor, radiographic-film, automatic
510(k) Number K001321
Device Name ALL-PRO 2010
Applicant
ALL-PRO IMAGING CORP.
70 CANTIAGUE ROCK RD.
P.O. BOX 870
HICKSVILLE,  NY  11801
Applicant Contact JOSEPH CAREY
Correspondent
ALL-PRO IMAGING CORP.
70 CANTIAGUE ROCK RD.
P.O. BOX 870
HICKSVILLE,  NY  11801
Correspondent Contact JOSEPH CAREY
Regulation Number892.1900
Classification Product Code
IXW  
Date Received04/26/2000
Decision Date 05/16/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-